Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 135644 |
| ensemblid | ENSG00000204614.9 |
| hgncid | 18736 |
| symbol | TRIM40 |
| name | tripartite motif containing 40 |
| refseq_nuc | NM_001286633.2 |
| refseq_prot | NP_001273562.1 |
| ensembl_nuc | ENST00000396581.6 |
| ensembl_prot | ENSP00000379826.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 30136140 |
| end | 30148728 |
| strand | + |
| ver | v1.2 |
| region | chr6:30136140-30148728 |
| region5000 | chr6:30131140-30153728 |
| regionname0 | TRIM40_chr6_30136140_30148728 |
| regionname5000 | TRIM40_chr6_30131140_30153728 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 258 | 380 | 81 | 60 | 186 | 14 | 38 | 150 | TRIM40_chr6_30131140_30153728 | TRIM40 | MIPLQ others(253): Show |
chr6 | 30131140 | 30153728 |
| a0002 | 0/0 | 258 | 56 | 5 | 16 | 30 | 3 | 2 | 22 | TRIM40_chr6_30131140_30153728 | TRIM40 | MIPLQ others(253): Show |
chr6 | 30131140 | 30153728 |
| a0003 | 0/0 | 258 | 9 | 0 | 3 | 0 | 0 | 6 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | MIPLQ others(253): Show |
chr6 | 30131140 | 30153728 |
| a0004 | 0/0 | 258 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | MIPLQ others(253): Show |
chr6 | 30131140 | 30153728 |
| a0005 | 0/0 | 258 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | MIPLQ others(253): Show |
chr6 | 30131140 | 30153728 |
| a0006 | 0/0 | 258 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | MIPLQ others(253): Show |
chr6 | 30131140 | 30153728 |
| a0007 | 0/0 | 258 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | MIPLQ others(253): Show |
chr6 | 30131140 | 30153728 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 774 | 379 | 81 | 60 | 185 | 14 | 38 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 | ||
| a0001c0009 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 | ||
| a0002c0002 | 0/0 | 774 | 51 | 2 | 14 | 30 | 3 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 | ||
| a0002c0005 | 0/0 | 774 | 5 | 3 | 2 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 | ||
| a0003c0003 | 0/0 | 774 | 9 | 0 | 3 | 0 | 0 | 6 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 | ||
| a0004c0004 | 0/0 | 774 | 8 | 7 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 | ||
| a0005c0008 | 0/0 | 774 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 | ||
| a0006c0006 | 0/0 | 774 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 | ||
| a0007c0007 | 0/0 | 774 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | ATGAT others(769): Show |
chr6 | 30131140 | 30153728 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2047 | 212 | 30 | 35 | 115 | 12 | 20 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0002 | 0/0 | 2047 | 69 | 18 | 9 | 40 | 2 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0004 | 0/0 | 2047 | 21 | 0 | 6 | 14 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0005 | 0/1 | 2047 | 14 | 1 | 1 | 6 | 0 | 5 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0006 | 0/0 | 2047 | 16 | 14 | 0 | 1 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0007 | 0/0 | 2047 | 12 | 12 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0008 | 0/0 | 2047 | 11 | 0 | 8 | 2 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0011 | 0/0 | 2047 | 7 | 0 | 0 | 1 | 0 | 6 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0012 | 0/0 | 2047 | 6 | 3 | 1 | 0 | 0 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0013 | 0/0 | 2047 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0014 | 0/0 | 2047 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0015 | 0/0 | 2047 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0017 | 0/0 | 2047 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0018 | 0/0 | 2047 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0019 | 0/0 | 2047 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0020 | 0/0 | 2047 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0001t0022 | 0/0 | 2047 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0001c0009t0001 | 0/0 | 2047 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0002c0002t0003 | 0/0 | 2047 | 51 | 2 | 14 | 30 | 3 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0002c0005t0003 | 0/0 | 2047 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0002c0005t0021 | 0/0 | 2047 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0003c0003t0009 | 0/0 | 2047 | 9 | 0 | 3 | 0 | 0 | 6 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0004c0004t0010 | 0/0 | 2047 | 8 | 7 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0005c0008t0005 | 0/0 | 2047 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0006c0006t0016 | 0/0 | 2047 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| a0007c0007t0001 | 0/0 | 2047 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | AGGTC others(2042): Show |
chr6 | 30131140 | 30153728 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 40 | 0 | 6 | 27 | 2 | 5 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0005 | 0/0 | 19 | 0 | 0 | 15 | 2 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0007 | 0/0 | 16 | 9 | 0 | 5 | 0 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0008 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0010 | 0/0 | 15 | 2 | 6 | 5 | 0 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0011 | 0/0 | 10 | 5 | 2 | 0 | 0 | 3 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0012 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0013 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0017 | 0/0 | 7 | 1 | 5 | 0 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0018 | 0/0 | 5 | 1 | 1 | 2 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0019 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0002 | 0/0 | 27 | 3 | 2 | 22 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0006 | 0/0 | 19 | 3 | 0 | 16 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0016 | 0/0 | 9 | 1 | 6 | 0 | 2 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0004g0004 | 0/0 | 20 | 0 | 6 | 13 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0005g0009 | 0/1 | 13 | 1 | 1 | 5 | 0 | 5 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0006g0002 | 0/0 | 16 | 14 | 0 | 1 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0007g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0007g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0007g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0008g0014 | 0/0 | 10 | 0 | 8 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0011g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0011g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0011g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0012g0025 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0013g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0014g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0015g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0015g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0017g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0018g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0019g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0001t0022g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0001c0009t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0003 | 0/0 | 40 | 1 | 13 | 23 | 2 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0005t0003g0031 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0005t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0002c0005t0021g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0003c0003t0009g0015 | 0/0 | 9 | 0 | 3 | 0 | 0 | 6 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0004c0004t0010g0020 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0004c0004t0010g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0004c0004t0010g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0005c0008t0005g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0006c0006t0016g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0006c0006t0016g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| a0007c0007t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00140 | hp1 | a0002 | c0002 | t0003 | g0003 | EUR | GBR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00140 | hp2 | a0005 | c0008 | t0005 | g0009 | EUR | GBR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0003 | EUR | FIN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00323 | hp1 | a0002 | c0002 | t0003 | g0107 | EUR | FIN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00609 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00621 | hp1 | a0002 | c0002 | t0003 | g0102 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00639 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00673 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | CHS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00738 | hp2 | a0003 | c0003 | t0009 | g0015 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01109 | hp1 | a0003 | c0003 | t0009 | g0015 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01243 | hp2 | a0004 | c0004 | t0010 | g0020 | AMR | PUR | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01255 | hp1 | a0002 | c0005 | t0021 | g0103 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01255 | hp2 | a0002 | c0005 | t0003 | g0031 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01256 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01257 | hp1 | a0001 | c0001 | t0012 | g0025 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0014 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01258 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0014 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0054 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01952 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01975 | hp1 | a0003 | c0003 | t0009 | g0015 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01978 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02015 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0100 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02074 | hp2 | a0001 | c0001 | t0011 | g0043 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02145 | hp2 | a0002 | c0005 | t0003 | g0031 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02148 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02165 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | CDX | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0048 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02273 | hp1 | a0002 | c0002 | t0003 | g0101 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0055 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02602 | hp1 | a0003 | c0003 | t0009 | g0015 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02602 | hp2 | a0006 | c0006 | t0016 | g0088 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02630 | hp1 | a0004 | c0004 | t0010 | g0020 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02683 | hp1 | a0002 | c0002 | t0003 | g0111 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02698 | hp1 | a0001 | c0001 | t0012 | g0025 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02723 | hp1 | a0004 | c0004 | t0010 | g0041 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0023 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02738 | hp1 | a0001 | c0001 | t0022 | g0049 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02809 | hp2 | a0004 | c0004 | t0010 | g0041 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02886 | hp1 | a0004 | c0004 | t0010 | g0115 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0109 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02970 | hp1 | a0004 | c0004 | t0010 | g0020 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0060 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03017 | hp2 | a0001 | c0001 | t0011 | g0032 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03098 | hp2 | a0004 | c0004 | t0010 | g0020 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03209 | hp2 | a0002 | c0005 | t0003 | g0031 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03490 | hp1 | a0003 | c0003 | t0009 | g0015 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03492 | hp1 | a0003 | c0003 | t0009 | g0015 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03540 | hp1 | a0006 | c0006 | t0016 | g0089 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03579 | hp2 | a0001 | c0001 | t0019 | g0011 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0023 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03669 | hp1 | a0003 | c0003 | t0009 | g0015 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03688 | hp2 | a0003 | c0003 | t0009 | g0015 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0023 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03834 | hp1 | a0001 | c0001 | t0018 | g0009 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03942 | hp1 | a0003 | c0003 | t0009 | g0015 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | BEB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0098 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04228 | hp1 | a0001 | c0001 | t0011 | g0032 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG04228 | hp2 | a0005 | c0008 | t0005 | g0009 | SAS | STU | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18522 | hp1 | a0004 | c0004 | t0010 | g0020 | AFR | YRI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | YRI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | CHB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | CHB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18961 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18963 | hp2 | a0001 | c0009 | t0001 | g0029 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18967 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18967 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18969 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18970 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18971 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18972 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18975 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18980 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18981 | hp2 | a0007 | c0007 | t0001 | g0029 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18983 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18991 | hp1 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18997 | hp1 | a0001 | c0001 | t0017 | g0091 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19002 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19010 | hp2 | a0001 | c0001 | t0014 | g0084 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0099 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19030 | hp2 | a0002 | c0005 | t0003 | g0110 | AFR | LWK | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19063 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19063 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19076 | hp1 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19080 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19084 | hp1 | a0007 | c0007 | t0001 | g0029 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | YRI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | YRI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | ASW | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20905 | hp1 | a0001 | c0001 | t0011 | g0042 | SAS | GIH | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20905 | hp2 | a0001 | c0001 | t0012 | g0025 | SAS | GIH | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | MSL | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | USA | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | USA | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | USA | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0003 | AFR | USA | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA21309 | hp1 | a0001 | c0001 | t0015 | g0082 | AFR | LWK | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0009 | REF | REF | TRIM40_chr6_30131140_30153728 | TRIM40 | chr6 | 30131140 | 30153728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30137212 | C | A | 1 | a0006 | 2 | HG02602.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.176C>A | p.Pro59His | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 530/2047 | 176/777 | 59/258 | chr6 | 30137212 | |||
| chr6:30137336 | G | C | 1 | a0004 | 8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.300G>C | p.Met100Ile | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 654/2047 | 300/777 | 100/258 | chr6 | 30137336 | |||
| chr6:30137377 | A | G | 1 | a0005 | 2 | HG00140.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.341A>G | p.Tyr114Cys | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 695/2047 | 341/777 | 114/258 | chr6 | 30137377 | |||
| chr6:30147048 | G | A | 1 | a0003 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
missense_variant | MODERATE | c.505G>A | p.Glu169Lys | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/6 | 859/2047 | 505/777 | 169/258 | chr6 | 30147048 | |||
| chr6:30147120 | C | T | 1 | a0003 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
missense_variant | MODERATE | c.577C>T | p.Leu193Phe | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/6 | 931/2047 | 577/777 | 193/258 | chr6 | 30147120 | |||
| chr6:30147178 | C | T | 2 | a0002 a0004 |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
missense_variant | MODERATE | c.635C>T | p.Thr212Met | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/6 | 989/2047 | 635/777 | 212/258 | chr6 | 30147178 | |||
| chr6:30147765 | G | A | 2 | a0002 a0004 |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
missense_variant | MODERATE | c.730G>A | p.Glu244Lys | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 1084/2047 | 730/777 | 244/258 | chr6 | 30147765 | |||
| chr6:30147768 | A | C | 1 | a0007 | 2 | NA18981.hp2 NA19084.hp1 |
missense_variant | MODERATE | c.733A>C | p.Lys245Gln | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 1087/2047 | 733/777 | 245/258 | chr6 | 30147768 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30137195 | C | T | 1 | a0004c0004 | 8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
synonymous_variant | LOW | c.159C>T | p.Cys53Cys | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 513/2047 | 159/777 | 53/258 | chr6 | 30137195 | |||
| chr6:30137219 | T | C | 1 | a0004c0004 | 8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
synonymous_variant | LOW | c.183T>C | p.Ser61Ser | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 537/2047 | 183/777 | 61/258 | chr6 | 30137219 | |||
| chr6:30147026 | G | A | 2 | a0003c0003 a0006c0006 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
synonymous_variant | LOW | c.483G>A | p.Pro161Pro | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/6 | 837/2047 | 483/777 | 161/258 | chr6 | 30147026 | |||
| chr6:30147068 | T | C | 1 | a0002c0002 | 51 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(48): Show |
synonymous_variant | LOW | c.525T>C | p.Pro175Pro | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/6 | 879/2047 | 525/777 | 175/258 | chr6 | 30147068 | |||
| chr6:30147156 | C | T | 1 | a0001c0009 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.613C>T | p.Leu205Leu | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/6 | 967/2047 | 613/777 | 205/258 | chr6 | 30147156 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30136146 | G | A | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(3): Show |
102 | HG00140.hp2 HG00558.hp1 HG00741.hp2 others(99): Show |
5_prime_UTR_variant | MODIFIER | c.-348G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/6 | 891 | chr6 | 30136146 | ||||||
| chr6:30136166 | G | C | 1 | a0001c0001t0012 | 6 | HG01257.hp1 HG01884.hp2 HG02257.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-328G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/6 | 871 | chr6 | 30136166 | ||||||
| chr6:30136764 | C | T | 1 | a0004c0004t0010 | 8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-273C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 273 | chr6 | 30136764 | ||||||
| chr6:30136816 | C | T | 1 | a0001c0001t0018 | 1 | HG03834.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-221C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | chr6 | 30136816 | |||||||
| chr6:30136820 | C | A | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(3): Show |
102 | HG00140.hp2 HG00558.hp1 HG00741.hp2 others(99): Show |
5_prime_UTR_variant | MODIFIER | c.-217C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 217 | chr6 | 30136820 | ||||||
| chr6:30136972 | C | A | 1 | a0004c0004t0010 | 8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 65 | chr6 | 30136972 | ||||||
| chr6:30136976 | C | T | 1 | a0004c0004t0010 | 8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-61C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 61 | chr6 | 30136976 | ||||||
| chr6:30136977 | C | T | 1 | a0004c0004t0010 | 8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | chr6 | 30136977 | |||||||
| chr6:30137006 | A | G | 10 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(7): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
5_prime_UTR_variant | MODIFIER | c.-31A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 31 | chr6 | 30137006 | ||||||
| chr6:30137031 | G | A | 4 | a0001c0001t0011 a0002c0002t0003 a0002c0005t0003 others(1): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-6G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/6 | 6 | chr6 | 30137031 | ||||||
| chr6:30147851 | C | T | 1 | a0002c0005t0021 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 39 | chr6 | 30147851 | ||||||
| chr6:30147923 | C | T | 1 | a0001c0001t0015 | 2 | HG02976.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 111 | chr6 | 30147923 | ||||||
| chr6:30147996 | C | T | 2 | a0001c0001t0006 a0004c0004t0010 |
24 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*184C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 184 | chr6 | 30147996 | ||||||
| chr6:30148062 | G | C | 1 | a0001c0001t0019 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 250 | chr6 | 30148062 | ||||||
| chr6:30148169 | G | A | 3 | a0001c0001t0005 a0001c0001t0018 a0005c0008t0005 |
16 | HG00140.hp2 HG00558.hp1 HG01074.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*357G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 357 | chr6 | 30148169 | ||||||
| chr6:30148188 | C | T | 4 | a0002c0002t0003 a0002c0005t0003 a0002c0005t0021 others(1): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*376C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 376 | chr6 | 30148188 | ||||||
| chr6:30148251 | C | T | 1 | a0001c0001t0022 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 439 | chr6 | 30148251 | ||||||
| chr6:30148272 | G | A | 2 | a0001c0001t0004 a0001c0001t0020 |
22 | HG00673.hp1 HG01167.hp1 HG01168.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*460G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 460 | chr6 | 30148272 | ||||||
| chr6:30148301 | A | G | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(19): Show |
428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
3_prime_UTR_variant | MODIFIER | c.*489A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 489 | chr6 | 30148301 | ||||||
| chr6:30148317 | G | A | 2 | a0001c0001t0013 a0001c0001t0020 |
3 | NA18967.hp1 NA18983.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*505G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 505 | chr6 | 30148317 | ||||||
| chr6:30148383 | G | C | 7 | a0001c0001t0011 a0002c0002t0003 a0002c0005t0003 others(4): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*571G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 571 | chr6 | 30148383 | ||||||
| chr6:30148414 | A | G | 1 | a0001c0001t0014 | 2 | NA18971.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*602A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 602 | chr6 | 30148414 | ||||||
| chr6:30148426 | G | A | 1 | a0006c0006t0016 | 2 | HG02602.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*614G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 614 | chr6 | 30148426 | ||||||
| chr6:30148487 | C | G | 1 | a0003c0003t0009 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*675C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 675 | chr6 | 30148487 | ||||||
| chr6:30148564 | C | T | 4 | a0002c0002t0003 a0002c0005t0003 a0002c0005t0021 others(1): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*752C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 752 | chr6 | 30148564 | ||||||
| chr6:30148625 | C | T | 1 | a0001c0001t0017 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 813 | chr6 | 30148625 | ||||||
| chr6:30148708 | A | G | 1 | a0001c0001t0011 | 7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*896A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 6/6 | 896 | chr6 | 30148708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30136198 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-305+9C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136198 | |||||||
| chr6:30136290 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-305+101C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136290 | |||||||
| chr6:30136291 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-305+102G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136291 | |||||||
| chr6:30136301 | T | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-305+112T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136301 | |||||||
| chr6:30136357 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-305+168C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136357 | |||||||
| chr6:30136373 | A | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-305+184A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136373 | |||||||
| chr6:30136519 | G | A | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-304-214G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136519 | |||||||
| chr6:30136526 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-304-207C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136526 | |||||||
| chr6:30136597 | T | C | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.-304-136T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136597 | |||||||
| chr6:30136626 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-304-107C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136626 | |||||||
| chr6:30136630 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
19 | HG02015.hp1 HG02055.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.-304-103G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136630 | |||||||
| chr6:30136677 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-304-56C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136677 | |||||||
| chr6:30136703 | A | G | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.-304-30A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136703 | |||||||
| chr6:30136712 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-304-21T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 1/5 | chr6 | 30136712 | |||||||
| chr6:30137397 | C | T | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.345+16C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137397 | |||||||
| chr6:30137430 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+49G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137430 | |||||||
| chr6:30137432 | T | A | 12 | a0001c0001t0007g0024 a0001c0001t0007g0026 a0001c0001t0007g0033 others(9): Show |
19 | HG01257.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.345+51T>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137432 | |||||||
| chr6:30137486 | T | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+105T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137486 | |||||||
| chr6:30137572 | T | C | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.345+191T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137572 | |||||||
| chr6:30137595 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+214G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137595 | |||||||
| chr6:30137614 | T | C | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+233T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137614 | |||||||
| chr6:30137642 | T | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+261T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137642 | |||||||
| chr6:30137649 | A | T | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.345+268A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137649 | |||||||
| chr6:30137741 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
20 | NA18940.hp1 NA18947.hp2 NA18950.hp1 others(17): Show |
intron_variant | MODIFIER | c.345+360T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137741 | |||||||
| chr6:30137767 | C | A | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.345+386C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137767 | |||||||
| chr6:30137799 | A | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+418A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137799 | |||||||
| chr6:30137801 | T | A | 1 | a0002c0002t0003g0099 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.345+420T>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137801 | |||||||
| chr6:30137810 | CTTTT | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+431_345+434del others(4): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30137810 | ||||||
| chr6:30137832 | T | C | 1 | a0002c0002t0003g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.345+451T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137832 | |||||||
| chr6:30137855 | T | C | 1 | a0001c0001t0015g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.345+474T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137855 | |||||||
| chr6:30137929 | C | A | 1 | a0002c0002t0003g0101 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.345+548C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137929 | |||||||
| chr6:30137966 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(99): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.345+585T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30137966 | |||||||
| chr6:30138066 | T | TAC | 15 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0062 others(12): Show |
102 | HG00621.hp2 HG00673.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.345+708_345+709dup others(2): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30138066 | ||||||
| chr6:30138066 | T | TACAC | 2 | a0001c0001t0001g0021 a0001c0001t0004g0061 |
5 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.345+706_345+709dup others(4): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30138066 | ||||||
| chr6:30138066 | TAC | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0090 a0001c0001t0011g0023 others(4): Show |
22 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.345+708_345+709del others(2): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30138066 | ||||||
| chr6:30138066 | TACACAC | T | 18 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(15): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.345+704_345+709del others(6): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30138066 | ||||||
| chr6:30138081 | A | C | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.345+700A>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138081 | |||||||
| chr6:30138085 | A | T | 1 | a0001c0001t0001g0039 | 2 | HG00609.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.345+704A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138085 | |||||||
| chr6:30138109 | A | C | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.345+728A>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138109 | |||||||
| chr6:30138127 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+746C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138127 | |||||||
| chr6:30138139 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+758C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138139 | |||||||
| chr6:30138147 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+766G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138147 | |||||||
| chr6:30138200 | G | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+819G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138200 | |||||||
| chr6:30138215 | A | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+834A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138215 | |||||||
| chr6:30138247 | A | T | 19 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(16): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.345+866A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138247 | |||||||
| chr6:30138254 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+873C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138254 | |||||||
| chr6:30138271 | T | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+890T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138271 | |||||||
| chr6:30138282 | A | T | 2 | a0001c0001t0004g0004 a0001c0001t0004g0061 |
21 | HG00673.hp1 HG01167.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.345+901A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138282 | |||||||
| chr6:30138293 | C | T | 37 | a0001c0001t0007g0024 a0001c0001t0007g0026 a0001c0001t0007g0033 others(34): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.345+912C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138293 | |||||||
| chr6:30138294 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
20 | HG02015.hp1 HG02055.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.345+913G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138294 | |||||||
| chr6:30138309 | C | T | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.345+928C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138309 | |||||||
| chr6:30138425 | G | A | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+1044G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138425 | |||||||
| chr6:30138443 | T | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1062T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138443 | |||||||
| chr6:30138477 | T | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1096T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138477 | |||||||
| chr6:30138481 | A | G | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.345+1100A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138481 | |||||||
| chr6:30138504 | C | G | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.345+1123C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138504 | |||||||
| chr6:30138504 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1123C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138504 | |||||||
| chr6:30138519 | G | A | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.345+1138G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138519 | |||||||
| chr6:30138643 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1262C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138643 | |||||||
| chr6:30138657 | T | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1276T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138657 | |||||||
| chr6:30138660 | A | G | 1 | a0002c0002t0003g0111 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.345+1279A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138660 | |||||||
| chr6:30138661 | T | A | 1 | a0001c0001t0011g0042 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.345+1280T>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138661 | |||||||
| chr6:30138672 | C | T | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.345+1291C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138672 | |||||||
| chr6:30138716 | T | C | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+1335T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138716 | |||||||
| chr6:30138723 | G | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1342G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138723 | |||||||
| chr6:30138747 | C | G | 1 | a0001c0001t0002g0093 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.345+1366C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30138747 | |||||||
| chr6:30139001 | G | A | 1 | a0001c0001t0012g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.345+1620G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139001 | |||||||
| chr6:30139118 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.345+1737C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139118 | |||||||
| chr6:30139193 | TA | T | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.345+1817delA | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30139193 | ||||||
| chr6:30139198 | A | C | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.345+1817A>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139198 | |||||||
| chr6:30139203 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1822G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139203 | |||||||
| chr6:30139330 | C | CT | 2 | a0003c0003t0009g0015 a0006c0006t0016g0089 |
10 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.345+1957dupT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30139330 | ||||||
| chr6:30139337 | TTC | T | 6 | a0001c0001t0007g0024 a0001c0001t0007g0033 a0001c0001t0007g0050 others(3): Show |
9 | HG02145.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.345+1958_345+1959d others(4): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30139337 | ||||||
| chr6:30139338 | TC | T | 17 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(14): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.345+1958delC | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139338 | |||||||
| chr6:30139339 | C | CT | 7 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0039 others(4): Show |
10 | HG01175.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.345+1980dupT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30139339 | ||||||
| chr6:30139339 | C | T | 3 | a0002c0002t0003g0102 a0002c0005t0021g0103 a0006c0006t0016g0088 |
3 | HG00621.hp1 HG01255.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.345+1958C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139339 | |||||||
| chr6:30139339 | CT | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(13): Show |
35 | HG00735.hp2 HG01106.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.345+1980delT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30139339 | ||||||
| chr6:30139339 | CTT | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0012g0055 |
6 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.345+1979_345+1980d others(4): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30139339 | ||||||
| chr6:30139339 | CTTTTTTT | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+1974_345+1980d others(9): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30139339 | ||||||
| chr6:30139340 | T | C | 9 | a0001c0001t0007g0024 a0001c0001t0007g0033 a0001c0001t0007g0050 others(6): Show |
12 | HG00621.hp1 HG01255.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.345+1959T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139340 | |||||||
| chr6:30139341 | T | C | 17 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(14): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.345+1960T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139341 | |||||||
| chr6:30139345 | T | C | 1 | a0001c0001t0002g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.345+1964T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139345 | |||||||
| chr6:30139346 | T | C | 1 | a0001c0001t0007g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.345+1965T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139346 | |||||||
| chr6:30139347 | T | C | 5 | a0002c0002t0003g0102 a0002c0005t0021g0103 a0004c0004t0010g0020 others(2): Show |
10 | HG00621.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.345+1966T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139347 | |||||||
| chr6:30139348 | T | C | 17 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(14): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.345+1967T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139348 | |||||||
| chr6:30139376 | T | C | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+1995T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139376 | |||||||
| chr6:30139388 | A | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+2007A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139388 | |||||||
| chr6:30139414 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+2033G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139414 | |||||||
| chr6:30139429 | C | T | 6 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(3): Show |
9 | HG02074.hp2 HG02602.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.345+2048C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139429 | |||||||
| chr6:30139500 | G | A | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.345+2119G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139500 | |||||||
| chr6:30139532 | A | G | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+2151A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139532 | |||||||
| chr6:30139691 | G | A | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.345+2310G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139691 | |||||||
| chr6:30139837 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+2456C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139837 | |||||||
| chr6:30139985 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+2604G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30139985 | |||||||
| chr6:30140029 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.345+2648T>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140029 | |||||||
| chr6:30140270 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+2889C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140270 | |||||||
| chr6:30140271 | G | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+2890G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140271 | |||||||
| chr6:30140298 | T | C | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.345+2917T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140298 | |||||||
| chr6:30140334 | C | T | 19 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(16): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.345+2953C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140334 | |||||||
| chr6:30140373 | T | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+2992T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140373 | |||||||
| chr6:30140425 | G | A | 12 | a0001c0001t0007g0024 a0001c0001t0007g0026 a0001c0001t0007g0033 others(9): Show |
19 | HG01257.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.345+3044G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140425 | |||||||
| chr6:30140528 | C | T | 2 | a0002c0005t0021g0103 a0003c0003t0009g0015 |
10 | HG00738.hp2 HG01109.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.345+3147C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140528 | |||||||
| chr6:30140530 | T | G | 1 | a0001c0001t0017g0091 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.345+3149T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140530 | |||||||
| chr6:30140532 | G | A | 1 | a0001c0001t0017g0091 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.345+3151G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140532 | |||||||
| chr6:30140533 | A | C | 1 | a0001c0001t0017g0091 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.345+3152A>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140533 | |||||||
| chr6:30140559 | A | G | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+3178A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140559 | |||||||
| chr6:30140573 | G | C | 1 | a0001c0001t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.345+3192G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140573 | |||||||
| chr6:30140615 | C | T | 12 | a0001c0001t0007g0024 a0001c0001t0007g0026 a0001c0001t0007g0033 others(9): Show |
19 | HG01257.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.345+3234C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140615 | |||||||
| chr6:30140657 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+3276G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140657 | |||||||
| chr6:30140657 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.345+3276G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140657 | |||||||
| chr6:30140682 | A | C | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.345+3301A>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140682 | |||||||
| chr6:30140691 | C | A | 25 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(22): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.345+3310C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140691 | |||||||
| chr6:30140767 | A | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+3386A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140767 | |||||||
| chr6:30140827 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.345+3446G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140827 | |||||||
| chr6:30140878 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+3497G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140878 | |||||||
| chr6:30140906 | C | T | 26 | a0001c0001t0008g0098 a0001c0001t0011g0023 a0001c0001t0011g0032 others(23): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.345+3525C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140906 | |||||||
| chr6:30140929 | T | C | 1 | a0001c0001t0012g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.345+3548T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140929 | |||||||
| chr6:30140974 | G | A | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+3593G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140974 | |||||||
| chr6:30140993 | C | A | 1 | a0001c0001t0012g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.345+3612C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140993 | |||||||
| chr6:30140993 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.345+3612C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30140993 | |||||||
| chr6:30141003 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+3622C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141003 | |||||||
| chr6:30141061 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.345+3680C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141061 | |||||||
| chr6:30141169 | C | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+3788C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141169 | |||||||
| chr6:30141169 | C | T | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.345+3788C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141169 | |||||||
| chr6:30141286 | G | A | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+3905G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141286 | |||||||
| chr6:30141351 | G | C | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.345+3970G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141351 | |||||||
| chr6:30141395 | GA | G | 22 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(19): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.345+4019delA | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30141395 | ||||||
| chr6:30141416 | G | A | 12 | a0001c0001t0007g0024 a0001c0001t0007g0026 a0001c0001t0007g0033 others(9): Show |
19 | HG01257.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.345+4035G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141416 | |||||||
| chr6:30141417 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.345+4036G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141417 | |||||||
| chr6:30141420 | C | T | 1 | a0001c0001t0014g0084 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.345+4039C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141420 | |||||||
| chr6:30141430 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG01123.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.345+4049C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141430 | |||||||
| chr6:30141484 | C | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.345+4103C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141484 | |||||||
| chr6:30141612 | G | C | 1 | a0001c0001t0011g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.345+4231G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141612 | |||||||
| chr6:30141635 | C | T | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.345+4254C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141635 | |||||||
| chr6:30141644 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.345+4263T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141644 | |||||||
| chr6:30141700 | T | G | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-4294T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141700 | |||||||
| chr6:30141705 | A | G | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.346-4289A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141705 | |||||||
| chr6:30141741 | A | G | 1 | a0006c0006t0016g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.346-4253A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141741 | |||||||
| chr6:30141956 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.346-4038C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141956 | |||||||
| chr6:30141996 | G | A | 4 | a0001c0001t0005g0009 a0001c0001t0005g0096 a0001c0001t0018g0009 others(1): Show |
16 | HG00140.hp2 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.346-3998G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30141996 | |||||||
| chr6:30142054 | T | C | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-3940T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142054 | |||||||
| chr6:30142072 | A | G | 1 | a0004c0004t0010g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.346-3922A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142072 | |||||||
| chr6:30142080 | C | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-3914C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142080 | |||||||
| chr6:30142084 | A | C | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-3910A>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142084 | |||||||
| chr6:30142102 | G | GT | 14 | a0001c0001t0001g0085 a0002c0002t0003g0003 a0002c0002t0003g0099 others(11): Show |
55 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.346-3883dupT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30142102 | ||||||
| chr6:30142109 | T | C | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-3885T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142109 | |||||||
| chr6:30142225 | G | T | 1 | a0001c0001t0001g0017 | 7 | HG00642.hp1 HG00733.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.346-3769G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142225 | |||||||
| chr6:30142256 | T | C | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-3738T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142256 | |||||||
| chr6:30142266 | T | A | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.346-3728T>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142266 | |||||||
| chr6:30142281 | G | A | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-3713G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142281 | |||||||
| chr6:30142335 | A | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-3659A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142335 | |||||||
| chr6:30142355 | A | T | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-3639A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142355 | |||||||
| chr6:30142437 | G | A | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-3557G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142437 | |||||||
| chr6:30142443 | A | C | 1 | a0001c0001t0015g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.346-3551A>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142443 | |||||||
| chr6:30142464 | A | G | 6 | a0003c0003t0009g0015 a0004c0004t0010g0020 a0004c0004t0010g0041 others(3): Show |
19 | HG00738.hp2 HG01109.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.346-3530A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142464 | |||||||
| chr6:30142560 | C | A | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-3434C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142560 | |||||||
| chr6:30142649 | G | T | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-3345G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142649 | |||||||
| chr6:30142734 | C | G | 1 | a0001c0001t0012g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.346-3260C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142734 | |||||||
| chr6:30142738 | G | A | 1 | a0001c0001t0012g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346-3256G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142738 | |||||||
| chr6:30142747 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
447 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(444): Show |
intron_variant | MODIFIER | c.346-3247C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142747 | |||||||
| chr6:30142784 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.346-3210T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142784 | |||||||
| chr6:30142811 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.346-3183C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142811 | |||||||
| chr6:30142824 | G | A | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-3170G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142824 | |||||||
| chr6:30142856 | G | GT | 4 | a0001c0001t0001g0080 a0004c0004t0010g0020 a0004c0004t0010g0041 others(1): Show |
9 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.346-3128dupT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30142856 | ||||||
| chr6:30142856 | G | T | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-3138G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142856 | |||||||
| chr6:30142900 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.346-3094A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142900 | |||||||
| chr6:30142911 | C | T | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.346-3083C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30142911 | |||||||
| chr6:30143014 | A | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-2980A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143014 | |||||||
| chr6:30143027 | T | G | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.346-2967T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143027 | |||||||
| chr6:30143040 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.346-2954C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143040 | |||||||
| chr6:30143081 | C | CTT | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-2912_346-2911i others(4): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30143081 | ||||||
| chr6:30143103 | G | A | 11 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(8): Show |
50 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.346-2891G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143103 | |||||||
| chr6:30143104 | TTTAG | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-2884_346-2881d others(6): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30143104 | ||||||
| chr6:30143146 | G | A | 1 | a0002c0005t0021g0103 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.346-2848G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143146 | |||||||
| chr6:30143237 | C | T | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-2757C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143237 | |||||||
| chr6:30143260 | T | C | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-2734T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143260 | |||||||
| chr6:30143294 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0063 |
17 | HG00621.hp2 HG00735.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.346-2700G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143294 | |||||||
| chr6:30143319 | A | T | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-2675A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143319 | |||||||
| chr6:30143320 | A | T | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-2674A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143320 | |||||||
| chr6:30143341 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.346-2653G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143341 | |||||||
| chr6:30143344 | C | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-2650C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143344 | |||||||
| chr6:30143407 | G | A | 4 | a0001c0001t0012g0025 a0001c0001t0012g0048 a0001c0001t0012g0054 others(1): Show |
6 | HG01257.hp1 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-2587G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143407 | |||||||
| chr6:30143431 | C | CT | 23 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(20): Show |
73 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.346-2546dupT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30143431 | ||||||
| chr6:30143431 | CT | C | 36 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0062 others(33): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.346-2546delT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30143431 | ||||||
| chr6:30143431 | CTTT | C | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.346-2548_346-2546d others(5): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30143431 | ||||||
| chr6:30143574 | C | T | 25 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(22): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.346-2420C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143574 | |||||||
| chr6:30143631 | C | A | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-2363C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143631 | |||||||
| chr6:30143660 | A | G | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-2334A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143660 | |||||||
| chr6:30143701 | T | C | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.346-2293T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143701 | |||||||
| chr6:30143707 | C | A | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-2287C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143707 | |||||||
| chr6:30143710 | A | G | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.346-2284A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143710 | |||||||
| chr6:30143749 | C | T | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-2245C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143749 | |||||||
| chr6:30143756 | C | CA | 3 | a0001c0001t0001g0057 a0006c0006t0016g0088 a0006c0006t0016g0089 |
3 | HG02602.hp2 HG03540.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.346-2233dupA | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30143756 | ||||||
| chr6:30143808 | T | C | 2 | a0001c0001t0007g0050 a0001c0001t0022g0049 |
2 | HG02738.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.346-2186T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143808 | |||||||
| chr6:30143833 | A | T | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-2161A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143833 | |||||||
| chr6:30143842 | TTCAG | T | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-2148_346-2145d others(6): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30143842 | ||||||
| chr6:30143900 | T | C | 1 | a0001c0001t0005g0096 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.346-2094T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143900 | |||||||
| chr6:30143950 | G | A | 1 | a0001c0001t0002g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.346-2044G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30143950 | |||||||
| chr6:30144086 | G | A | 18 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(15): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.346-1908G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144086 | |||||||
| chr6:30144087 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.346-1907T>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144087 | |||||||
| chr6:30144098 | T | G | 1 | a0001c0001t0007g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.346-1896T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144098 | |||||||
| chr6:30144099 | G | A | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-1895G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144099 | |||||||
| chr6:30144109 | C | CAG | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-1884_346-1883d others(4): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30144109 | ||||||
| chr6:30144155 | C | T | 19 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(16): Show |
73 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.346-1839C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144155 | |||||||
| chr6:30144165 | C | T | 1 | a0001c0001t0007g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.346-1829C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144165 | |||||||
| chr6:30144194 | T | C | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.346-1800T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144194 | |||||||
| chr6:30144374 | T | C | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-1620T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144374 | |||||||
| chr6:30144416 | C | G | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-1578C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144416 | |||||||
| chr6:30144420 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(24): Show |
99 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.346-1574C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144420 | |||||||
| chr6:30144631 | A | G | 18 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(15): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.346-1363A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144631 | |||||||
| chr6:30144675 | C | T | 1 | a0002c0005t0003g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346-1319C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144675 | |||||||
| chr6:30144689 | G | A | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-1305G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144689 | |||||||
| chr6:30144805 | C | T | 1 | a0001c0001t0001g0030 | 3 | HG02300.hp2 NA18955.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.346-1189C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144805 | |||||||
| chr6:30144846 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0035 others(9): Show |
36 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.346-1148G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144846 | |||||||
| chr6:30144850 | G | A | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-1144G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144850 | |||||||
| chr6:30144867 | C | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
21 | HG04115.hp1 NA18940.hp1 NA18947.hp2 others(18): Show |
intron_variant | MODIFIER | c.346-1127C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144867 | |||||||
| chr6:30144927 | T | C | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-1067T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30144927 | |||||||
| chr6:30145018 | G | A | 1 | a0001c0001t0001g0021 | 4 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.346-976G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145018 | |||||||
| chr6:30145129 | T | C | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-865T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145129 | |||||||
| chr6:30145202 | A | AT | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-790dupT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30145202 | ||||||
| chr6:30145204 | TA | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(27): Show |
104 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.346-778delA | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 30145204 | ||||||
| chr6:30145205 | A | T | 18 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(15): Show |
67 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.346-789A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145205 | |||||||
| chr6:30145339 | C | CT | 13 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(10): Show |
31 | HG00738.hp2 HG01109.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.346-655_346-654ins others(1): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145339 | |||||||
| chr6:30145468 | C | A | 14 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(11): Show |
55 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.346-526C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145468 | |||||||
| chr6:30145468 | C | T | 1 | a0001c0001t0022g0049 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.346-526C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145468 | |||||||
| chr6:30145532 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.346-462G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145532 | |||||||
| chr6:30145567 | C | T | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-427C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145567 | |||||||
| chr6:30145640 | C | T | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-354C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145640 | |||||||
| chr6:30145650 | C | A | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-344C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145650 | |||||||
| chr6:30145686 | T | G | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.346-308T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145686 | |||||||
| chr6:30145694 | G | A | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.346-300G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145694 | |||||||
| chr6:30145716 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.346-278G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145716 | |||||||
| chr6:30145773 | T | A | 1 | a0001c0001t0001g0027 | 3 | HG00639.hp2 HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.346-221T>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145773 | |||||||
| chr6:30145853 | G | T | 3 | a0001c0001t0007g0033 a0001c0001t0007g0051 a0001c0001t0007g0052 |
4 | HG02572.hp1 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-141G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145853 | |||||||
| chr6:30145953 | C | A | 4 | a0001c0001t0012g0025 a0001c0001t0012g0048 a0001c0001t0012g0054 others(1): Show |
6 | HG01257.hp1 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-41C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145953 | |||||||
| chr6:30145953 | C | G | 1 | a0002c0002t0003g0108 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.346-41C>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | chr6 | 30145953 | |||||||
| chr6:30146101 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0040 a0001c0001t0002g0047 others(4): Show |
49 | HG00741.hp2 HG01106.hp2 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.441+12G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146101 | |||||||
| chr6:30146139 | C | A | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.441+50C>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146139 | |||||||
| chr6:30146178 | A | G | 21 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(18): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.441+89A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146178 | |||||||
| chr6:30146222 | T | G | 1 | a0002c0005t0021g0103 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.441+133T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146222 | |||||||
| chr6:30146233 | G | A | 4 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(1): Show |
7 | HG02074.hp2 HG02735.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+144G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146233 | |||||||
| chr6:30146286 | A | G | 1 | a0001c0001t0011g0032 | 2 | HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.441+197A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146286 | |||||||
| chr6:30146297 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(24): Show |
98 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.441+208A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146297 | |||||||
| chr6:30146324 | G | A | 25 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(22): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.441+235G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146324 | |||||||
| chr6:30146336 | G | A | 1 | a0001c0001t0008g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.441+247G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146336 | |||||||
| chr6:30146419 | A | AT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
28 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+340dupT | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 30146419 | ||||||
| chr6:30146419 | A | ATT | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+339_441+340dup others(2): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 30146419 | ||||||
| chr6:30146439 | C | T | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.441+350C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146439 | |||||||
| chr6:30146443 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441+354G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146443 | |||||||
| chr6:30146450 | C | T | 1 | a0002c0002t0003g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+361C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146450 | |||||||
| chr6:30146501 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.441+412T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146501 | |||||||
| chr6:30146512 | C | T | 4 | a0001c0001t0005g0009 a0001c0001t0005g0096 a0001c0001t0018g0009 others(1): Show |
16 | HG00140.hp2 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+423C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146512 | |||||||
| chr6:30146530 | G | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0022 |
13 | HG01074.hp1 HG01099.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+441G>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146530 | |||||||
| chr6:30146588 | A | T | 17 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(14): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.442-397A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146588 | |||||||
| chr6:30146613 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.442-372A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146613 | |||||||
| chr6:30146625 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(85): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.442-360A>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146625 | |||||||
| chr6:30146633 | G | A | 1 | a0004c0004t0010g0041 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.442-352G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146633 | |||||||
| chr6:30146700 | C | T | 2 | a0001c0009t0001g0029 a0007c0007t0001g0029 |
3 | NA18963.hp2 NA18981.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.442-285C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146700 | |||||||
| chr6:30146701 | G | A | 1 | a0002c0002t0003g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.442-284G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146701 | |||||||
| chr6:30146702 | T | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0035 others(11): Show |
39 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.442-283T>C | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146702 | |||||||
| chr6:30146720 | C | T | 3 | a0004c0004t0010g0020 a0004c0004t0010g0041 a0004c0004t0010g0115 |
8 | HG01243.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-265C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146720 | |||||||
| chr6:30146749 | T | G | 1 | a0001c0001t0002g0092 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.442-236T>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146749 | |||||||
| chr6:30146804 | G | A | 1 | a0001c0001t0001g0028 | 3 | NA18960.hp2 NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.442-181G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146804 | |||||||
| chr6:30146846 | T | A | 25 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(22): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.442-139T>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146846 | |||||||
| chr6:30146889 | C | T | 18 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(15): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.442-96C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146889 | |||||||
| chr6:30146948 | A | G | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-37A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3/5 | chr6 | 30146948 | |||||||
| chr6:30147286 | G | A | 15 | a0002c0002t0003g0003 a0002c0002t0003g0099 a0002c0002t0003g0100 others(12): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.666+77G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/5 | chr6 | 30147286 | |||||||
| chr6:30147376 | G | A | 1 | a0003c0003t0009g0015 | 9 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-144G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/5 | chr6 | 30147376 | |||||||
| chr6:30147383 | G | A | 3 | a0003c0003t0009g0015 a0006c0006t0016g0088 a0006c0006t0016g0089 |
11 | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.667-137G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/5 | chr6 | 30147383 | |||||||
| chr6:30147427 | C | T | 2 | a0002c0002t0003g0107 a0002c0002t0003g0111 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.667-93C>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 4/5 | chr6 | 30147427 | |||||||
| chr6:30147543 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG00735.hp1 | splice_donor_variant&intron_variant | HIGH | c.689+1G>T | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 5/5 | chr6 | 30147543 | |||||||
| chr6:30147579 | A | G | 2 | a0006c0006t0016g0088 a0006c0006t0016g0089 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.689+37A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 5/5 | chr6 | 30147579 | |||||||
| chr6:30147631 | G | A | 4 | a0002c0005t0021g0103 a0003c0003t0009g0015 a0006c0006t0016g0088 others(1): Show |
12 | HG00738.hp2 HG01109.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.689+89G>A | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 5/5 | chr6 | 30147631 | |||||||
| chr6:30147707 | A | G | 25 | a0001c0001t0011g0023 a0001c0001t0011g0032 a0001c0001t0011g0042 others(22): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.690-18A>G | TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 5/5 | chr6 | 30147707 |