Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84649 |
| ensemblid | ENSG00000062282.15 |
| hgncid | 16940 |
| symbol | DGAT2 |
| name | diacylglycerol O-acyltransferase 2 |
| refseq_nuc | NM_032564.5 |
| refseq_prot | NP_115953.2 |
| ensembl_nuc | ENST00000228027.12 |
| ensembl_prot | ENSP00000228027.6 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 75768778 |
| end | 75801534 |
| strand | + |
| ver | v1.2 |
| region | chr11:75768778-75801534 |
| region5000 | chr11:75763778-75806534 |
| regionname0 | DGAT2_chr11_75768778_75801534 |
| regionname5000 | DGAT2_chr11_75763778_75806534 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 388 | 309 | 78 | 46 | 142 | 8 | 33 | 104 | DGAT2_chr11_75763778_75806534 | DGAT2 | MKTLI others(383): Show |
chr11 | 75763778 | 75806534 |
| a0002 | 0/0 | 388 | 9 | 8 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | MKTLI others(383): Show |
chr11 | 75763778 | 75806534 |
| a0003 | 0/0 | 388 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | DGAT2_chr11_75763778_75806534 | DGAT2 | MKTLI others(383): Show |
chr11 | 75763778 | 75806534 |
| a0004 | 0/0 | 388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | MKTLI others(383): Show |
chr11 | 75763778 | 75806534 |
| a0005 | 0/0 | 388 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | MKTLI others(383): Show |
chr11 | 75763778 | 75806534 |
| a0006 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | MKTLI others(383): Show |
chr11 | 75763778 | 75806534 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1164 | 295 | 70 | 45 | 138 | 7 | 33 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0001c0003 | 0/0 | 1164 | 8 | 7 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0001c0005 | 0/0 | 1164 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0001c0006 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0001c0008 | 0/0 | 1164 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0001c0011 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0002c0002 | 0/0 | 1164 | 9 | 8 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0003c0004 | 0/0 | 1164 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0004c0009 | 0/0 | 1164 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0005c0010 | 0/0 | 1164 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 | ||
| a0006c0007 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | ATGAA others(1159): Show |
chr11 | 75763778 | 75806534 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2407 | 181 | 37 | 33 | 80 | 6 | 23 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0002 | 0/0 | 2407 | 102 | 29 | 10 | 55 | 1 | 7 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0004 | 0/0 | 2407 | 2 | 0 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0005 | 0/0 | 2407 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0006 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0007 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0008 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0009 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0011 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0012 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0013 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0001t0014 | 0/0 | 2407 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0003t0002 | 0/0 | 2407 | 8 | 7 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0005t0001 | 0/0 | 2407 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0006t0001 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0008t0010 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0001c0011t0001 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0002c0002t0002 | 0/0 | 2407 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0002c0002t0003 | 0/0 | 2407 | 8 | 7 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0003c0004t0001 | 0/0 | 2407 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0004c0009t0001 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0005c0010t0001 | 0/0 | 2407 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| a0006c0007t0001 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | GCCGC others(2402): Show |
chr11 | 75763778 | 75806534 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 34 | 3 | 1 | 26 | 1 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0003 | 0/0 | 17 | 0 | 4 | 4 | 3 | 6 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0006 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0037 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0002 | 0/0 | 28 | 1 | 5 | 18 | 0 | 4 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0009g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0011g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0001t0014g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0003t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0003t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0005t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0008t0010g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0001c0011t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0002c0002t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0002c0002t0003g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0002c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0002c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0003c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0003c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0003c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0004c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0005c0010t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| a0006c0007t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | GBR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00621 | hp2 | a0001 | c0005 | t0001 | g0016 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00639 | hp2 | a0001 | c0001 | t0014 | g0081 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | CHS | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0067 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0166 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02145 | hp2 | a0002 | c0002 | t0003 | g0061 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02523 | hp2 | a0001 | c0005 | t0001 | g0016 | EAS | KHV | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02622 | hp2 | a0002 | c0002 | t0003 | g0059 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02630 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02698 | hp1 | a0004 | c0009 | t0001 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0062 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03041 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0060 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0068 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0111 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0027 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0006 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04228 | hp1 | a0005 | c0010 | t0001 | g0115 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | YRI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0090 | AFR | YRI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18939 | hp1 | a0006 | c0007 | t0001 | g0019 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18942 | hp1 | a0003 | c0004 | t0001 | g0110 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18971 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18984 | hp2 | a0003 | c0004 | t0001 | g0135 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18994 | hp1 | a0003 | c0004 | t0001 | g0103 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19002 | hp1 | a0001 | c0005 | t0001 | g0016 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0087 | AFR | LWK | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0027 | AFR | LWK | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19043 | hp1 | a0001 | c0011 | t0001 | g0008 | AFR | LWK | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0142 | AFR | YRI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | YRI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ASW | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA20752 | hp1 | a0001 | c0008 | t0010 | g0143 | EUR | TSI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | GIH | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | MSL | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | USA | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | USA | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | USA | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | USA | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0037 | REF | REF | DGAT2_chr11_75763778_75806534 | DGAT2 | chr11 | 75763778 | 75806534 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75769052 | G | A | 1 | a0003 | 3 | NA18942.hp1 NA18984.hp2 NA18994.hp1 |
missense_variant | MODERATE | c.61G>A | p.Asp21Asn | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | 275/2407 | 61/1167 | 21/388 | chr11 | 75769052 | |||
| chr11:75796340 | C | G | 1 | a0005 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.442C>G | p.His148Asp | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 5/8 | 656/2407 | 442/1167 | 148/388 | chr11 | 75796340 | |||
| chr11:75797224 | T | C | 1 | a0006 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.701T>C | p.Ile234Thr | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/8 | 915/2407 | 701/1167 | 234/388 | chr11 | 75797224 | |||
| chr11:75798267 | G | A | 1 | a0004 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.850G>A | p.Val284Met | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/8 | 1064/2407 | 850/1167 | 284/388 | chr11 | 75798267 | |||
| chr11:75800424 | G | A | 1 | a0002 | 9 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
missense_variant | MODERATE | c.1083G>A | p.Met361Ile | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 1297/2407 | 1083/1167 | 361/388 | chr11 | 75800424 | |||
| chr11:75801533 | T | C | 1 | a0001 | 1 | HG03491.hp1 | splice_region_variant | LOW | c.*1025T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | chr11 | 75801533 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75769063 | G | A | 1 | a0001c0003 | 8 | HG01074.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
synonymous_variant | LOW | c.72G>A | p.Gln24Gln | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | 286/2407 | 72/1167 | 24/388 | chr11 | 75769063 | |||
| chr11:75790210 | C | T | 1 | a0001c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.273C>T | p.Leu91Leu | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 3/8 | 487/2407 | 273/1167 | 91/388 | chr11 | 75790210 | |||
| chr11:75790710 | T | C | 1 | a0001c0006 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.408T>C | p.Phe136Phe | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/8 | 622/2407 | 408/1167 | 136/388 | chr11 | 75790710 | |||
| chr11:75797288 | C | A | 1 | a0001c0008 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.765C>A | p.Thr255Thr | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/8 | 979/2407 | 765/1167 | 255/388 | chr11 | 75797288 | |||
| chr11:75798344 | C | T | 1 | a0001c0005 | 3 | HG00621.hp2 HG02523.hp2 NA19002.hp1 |
synonymous_variant | LOW | c.927C>T | p.Phe309Phe | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/8 | 1141/2407 | 927/1167 | 309/388 | chr11 | 75798344 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75768789 | C | T | 1 | a0001c0001t0014 | 1 | HG00639.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-203C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | chr11 | 75768789 | |||||||
| chr11:75768817 | C | G | 1 | a0001c0001t0005 | 2 | HG00673.hp2 HG02083.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-175C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | chr11 | 75768817 | |||||||
| chr11:75768819 | C | T | 2 | a0001c0001t0013 a0002c0002t0003 |
9 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-173C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | chr11 | 75768819 | |||||||
| chr11:75768845 | G | C | 1 | a0001c0001t0006 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-147G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/8 | 147 | chr11 | 75768845 | ||||||
| chr11:75800527 | T | C | 8 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(5): Show |
123 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*19T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 19 | chr11 | 75800527 | ||||||
| chr11:75800707 | C | A | 1 | a0001c0001t0013 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 199 | chr11 | 75800707 | ||||||
| chr11:75800882 | C | G | 1 | a0001c0001t0007 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*374C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 374 | chr11 | 75800882 | ||||||
| chr11:75800917 | T | C | 1 | a0001c0001t0004 | 2 | HG01175.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*409T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 409 | chr11 | 75800917 | ||||||
| chr11:75801072 | C | T | 1 | a0001c0001t0012 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 564 | chr11 | 75801072 | ||||||
| chr11:75801224 | T | C | 1 | a0001c0001t0008 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*716T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 716 | chr11 | 75801224 | ||||||
| chr11:75801425 | G | A | 1 | a0001c0001t0009 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*917G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 917 | chr11 | 75801425 | ||||||
| chr11:75801488 | T | C | 1 | a0001c0008t0010 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 8/8 | 980 | chr11 | 75801488 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75769152 | A | G | 1 | a0001c0001t0001g0042 | 2 | NA18943.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.121+40A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769152 | |||||||
| chr11:75769325 | T | C | 6 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+213T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769325 | |||||||
| chr11:75769375 | C | G | 5 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+263C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769375 | |||||||
| chr11:75769410 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.121+298A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769410 | |||||||
| chr11:75769637 | G | T | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.121+525G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769637 | |||||||
| chr11:75769815 | C | G | 1 | a0001c0001t0002g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121+703C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769815 | |||||||
| chr11:75769819 | A | T | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+707A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75769819 | |||||||
| chr11:75770085 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.121+973A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770085 | |||||||
| chr11:75770141 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.121+1029A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770141 | |||||||
| chr11:75770286 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG00642.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.121+1174G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770286 | |||||||
| chr11:75770488 | G | C | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.121+1376G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770488 | |||||||
| chr11:75770619 | G | C | 75 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(72): Show |
132 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.121+1507G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770619 | |||||||
| chr11:75770799 | CT | C | 18 | a0001c0001t0001g0053 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
22 | HG00438.hp1 HG01243.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+1699delT | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75770799 | ||||||
| chr11:75770997 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.121+1885G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75770997 | |||||||
| chr11:75771053 | G | A | 1 | a0001c0001t0001g0034 | 2 | NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.121+1941G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771053 | |||||||
| chr11:75771221 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG00323.hp2 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.121+2109G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771221 | |||||||
| chr11:75771249 | T | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0057 |
3 | HG00642.hp2 HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.121+2137T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771249 | |||||||
| chr11:75771272 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.121+2160C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771272 | |||||||
| chr11:75771465 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121+2353A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771465 | |||||||
| chr11:75771793 | A | G | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+2681A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771793 | |||||||
| chr11:75771882 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.121+2770A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75771882 | |||||||
| chr11:75772040 | C | G | 1 | a0001c0001t0002g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.121+2928C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772040 | |||||||
| chr11:75772044 | T | G | 1 | a0001c0001t0002g0010 | 3 | HG01891.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.121+2932T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772044 | |||||||
| chr11:75772087 | G | A | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+2975G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772087 | |||||||
| chr11:75772099 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.121+2987G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772099 | |||||||
| chr11:75772166 | C | T | 2 | a0001c0001t0002g0167 a0001c0001t0007g0166 |
2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.121+3054C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772166 | |||||||
| chr11:75772518 | C | G | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.121+3406C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772518 | |||||||
| chr11:75772521 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+3409C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772521 | |||||||
| chr11:75772527 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+3415A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772527 | |||||||
| chr11:75772578 | A | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(32): Show |
65 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.121+3466A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772578 | |||||||
| chr11:75772623 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.121+3511A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772623 | |||||||
| chr11:75772682 | A | G | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+3570A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772682 | |||||||
| chr11:75772706 | G | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG02055.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.121+3594G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772706 | |||||||
| chr11:75772860 | T | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(55): Show |
108 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.121+3748T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772860 | |||||||
| chr11:75772967 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121+3855G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75772967 | |||||||
| chr11:75773224 | C | A | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.121+4112C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773224 | |||||||
| chr11:75773388 | C | G | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+4276C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773388 | |||||||
| chr11:75773734 | C | T | 6 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+4622C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773734 | |||||||
| chr11:75773805 | A | G | 34 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(31): Show |
82 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.121+4693A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773805 | |||||||
| chr11:75773884 | C | G | 27 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(24): Show |
71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.121+4772C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75773884 | |||||||
| chr11:75774150 | T | G | 1 | a0001c0001t0002g0069 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.121+5038T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774150 | |||||||
| chr11:75774186 | G | A | 30 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(27): Show |
74 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.121+5074G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774186 | |||||||
| chr11:75774265 | C | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
10 | HG02040.hp1 HG02071.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.121+5153C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774265 | |||||||
| chr11:75774293 | C | G | 1 | a0001c0001t0002g0069 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.121+5181C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774293 | |||||||
| chr11:75774321 | C | T | 1 | a0001c0008t0010g0143 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.121+5209C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774321 | |||||||
| chr11:75774427 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.121+5315T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774427 | |||||||
| chr11:75774452 | T | G | 1 | a0001c0001t0002g0172 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.121+5340T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774452 | |||||||
| chr11:75774494 | C | T | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.121+5382C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774494 | |||||||
| chr11:75774644 | G | T | 1 | a0001c0001t0012g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.121+5532G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774644 | |||||||
| chr11:75774758 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.121+5646C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75774758 | |||||||
| chr11:75775195 | C | T | 1 | a0001c0001t0001g0034 | 2 | NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.121+6083C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775195 | |||||||
| chr11:75775239 | GAAGAGGC others(9): Show |
G | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.121+6128_121+6143d others(18): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775239 | |||||||
| chr11:75775251 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.121+6139C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775251 | |||||||
| chr11:75775427 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG02818.hp1 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.121+6315T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775427 | |||||||
| chr11:75775542 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.121+6430G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75775542 | |||||||
| chr11:75776001 | C | A | 1 | a0001c0001t0002g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.121+6889C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776001 | |||||||
| chr11:75776100 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121+6988C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776100 | |||||||
| chr11:75776101 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.121+6989G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776101 | |||||||
| chr11:75776111 | A | G | 2 | a0001c0001t0001g0008 a0001c0011t0001g0008 |
4 | HG02258.hp2 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+6999A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776111 | |||||||
| chr11:75776243 | A | C | 2 | a0001c0003t0002g0067 a0001c0003t0002g0068 |
2 | HG01074.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.121+7131A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776243 | |||||||
| chr11:75776277 | C | T | 24 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0039 others(21): Show |
29 | HG00597.hp1 HG00642.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.121+7165C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776277 | |||||||
| chr11:75776281 | C | T | 31 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(28): Show |
75 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.121+7169C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776281 | |||||||
| chr11:75776429 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0007g0166 |
2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.121+7317A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776429 | |||||||
| chr11:75776566 | A | G | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.121+7454A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776566 | |||||||
| chr11:75776601 | C | G | 2 | a0001c0001t0002g0029 a0001c0001t0002g0091 |
3 | HG02451.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.121+7489C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75776601 | |||||||
| chr11:75777006 | G | A | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-7612G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777006 | |||||||
| chr11:75777009 | C | A | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(21): Show |
67 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.122-7609C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777009 | |||||||
| chr11:75777115 | G | C | 1 | a0001c0001t0001g0040 | 2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.122-7503G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777115 | |||||||
| chr11:75777141 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.122-7477C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777141 | |||||||
| chr11:75777294 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.122-7324G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777294 | |||||||
| chr11:75777312 | CAG | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0094 |
4 | NA18939.hp2 NA18956.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-7305_122-7304d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777312 | |||||||
| chr11:75777723 | G | C | 1 | a0001c0001t0014g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.122-6895G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777723 | |||||||
| chr11:75777802 | C | T | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.122-6816C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75777802 | |||||||
| chr11:75778045 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-6573T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778045 | |||||||
| chr11:75778076 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-6542T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778076 | |||||||
| chr11:75778185 | A | G | 1 | a0001c0001t0002g0028 | 2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.122-6433A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778185 | |||||||
| chr11:75778283 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.122-6335C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778283 | |||||||
| chr11:75778284 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0101 a0001c0001t0001g0102 |
5 | HG01123.hp2 HG01192.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-6334G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778284 | |||||||
| chr11:75778310 | A | T | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-6308A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778310 | |||||||
| chr11:75778359 | C | A | 30 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(27): Show |
74 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.122-6259C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778359 | |||||||
| chr11:75778364 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122-6254C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778364 | |||||||
| chr11:75778525 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-6093C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778525 | |||||||
| chr11:75778527 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-6091T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778527 | |||||||
| chr11:75778561 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.122-6057G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778561 | |||||||
| chr11:75778675 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.122-5943A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778675 | |||||||
| chr11:75778681 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-5937A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778681 | |||||||
| chr11:75778704 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122-5914G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778704 | |||||||
| chr11:75778767 | G | A | 3 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG00438.hp1 NA18951.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.122-5851G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778767 | |||||||
| chr11:75778833 | C | CA | 39 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(36): Show |
50 | HG00438.hp1 HG00438.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.122-5763dupA | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75778833 | ||||||
| chr11:75778833 | C | CAA | 25 | a0001c0001t0001g0082 a0001c0001t0002g0002 a0001c0001t0002g0004 others(22): Show |
67 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.122-5764_122-5763d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75778833 | ||||||
| chr11:75778833 | CA | C | 22 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0140 others(19): Show |
24 | HG01255.hp1 HG01255.hp2 HG02132.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-5763delA | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75778833 | ||||||
| chr11:75778985 | C | T | 1 | a0002c0002t0003g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.122-5633C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75778985 | |||||||
| chr11:75779093 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-5525G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779093 | |||||||
| chr11:75779109 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.122-5509G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779109 | |||||||
| chr11:75779154 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG00741.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.122-5464C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779154 | |||||||
| chr11:75779256 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-5362A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779256 | |||||||
| chr11:75779260 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-5358G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779260 | |||||||
| chr11:75779263 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.122-5355G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779263 | |||||||
| chr11:75779551 | C | A | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.122-5067C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779551 | |||||||
| chr11:75779572 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-5046C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779572 | |||||||
| chr11:75779597 | C | T | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.122-5021C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779597 | |||||||
| chr11:75779606 | C | A | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-5012C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779606 | |||||||
| chr11:75779660 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-4958A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779660 | |||||||
| chr11:75779775 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-4843C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779775 | |||||||
| chr11:75779843 | C | T | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-4775C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779843 | |||||||
| chr11:75779881 | C | CCCAGTCT others(10): Show |
1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-4736_122-4720d others(19): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75779881 | ||||||
| chr11:75779906 | C | A | 3 | a0001c0001t0002g0056 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-4712C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779906 | |||||||
| chr11:75779906 | C | G | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.122-4712C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75779906 | |||||||
| chr11:75780215 | T | A | 1 | a0002c0002t0002g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122-4403T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780215 | |||||||
| chr11:75780259 | C | T | 2 | a0001c0001t0002g0004 a0001c0001t0002g0088 |
7 | HG01192.hp1 NA18946.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-4359C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780259 | |||||||
| chr11:75780434 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0132 |
3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.122-4184C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780434 | |||||||
| chr11:75780451 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0101 a0001c0001t0001g0102 |
5 | HG01123.hp2 HG01192.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-4167C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780451 | |||||||
| chr11:75780479 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.122-4139G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780479 | |||||||
| chr11:75780732 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0094 |
4 | NA18939.hp2 NA18956.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-3886G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780732 | |||||||
| chr11:75780851 | A | G | 3 | a0001c0001t0002g0056 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-3767A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780851 | |||||||
| chr11:75780918 | T | A | 1 | a0001c0001t0006g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.122-3700T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780918 | |||||||
| chr11:75780930 | C | T | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122-3688C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780930 | |||||||
| chr11:75780959 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0082 others(1): Show |
6 | HG02622.hp1 HG02895.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-3659C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75780959 | |||||||
| chr11:75781029 | C | T | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-3589C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781029 | |||||||
| chr11:75781045 | G | A | 3 | a0001c0001t0002g0056 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-3573G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781045 | |||||||
| chr11:75781158 | T | C | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.122-3460T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781158 | |||||||
| chr11:75781382 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.122-3236G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781382 | |||||||
| chr11:75781484 | TG | T | 2 | a0001c0001t0002g0004 a0001c0001t0002g0088 |
7 | HG01192.hp1 NA18946.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-3131delG | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 75781484 | ||||||
| chr11:75781759 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.122-2859G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781759 | |||||||
| chr11:75781987 | A | C | 1 | a0002c0002t0003g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122-2631A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75781987 | |||||||
| chr11:75782024 | C | T | 7 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-2594C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782024 | |||||||
| chr11:75782089 | A | G | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.122-2529A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782089 | |||||||
| chr11:75782133 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.122-2485G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782133 | |||||||
| chr11:75782159 | C | T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-2459C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782159 | |||||||
| chr11:75782164 | A | G | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.122-2454A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782164 | |||||||
| chr11:75782295 | C | G | 1 | a0001c0001t0002g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122-2323C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782295 | |||||||
| chr11:75782338 | G | A | 3 | a0003c0004t0001g0103 a0003c0004t0001g0110 a0003c0004t0001g0135 |
3 | NA18942.hp1 NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.122-2280G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782338 | |||||||
| chr11:75782691 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.122-1927A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782691 | |||||||
| chr11:75782692 | A | G | 3 | a0001c0001t0002g0044 a0001c0001t0002g0046 a0001c0001t0002g0047 |
3 | HG01243.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.122-1926A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782692 | |||||||
| chr11:75782820 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.122-1798G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782820 | |||||||
| chr11:75782849 | T | C | 1 | a0001c0001t0004g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.122-1769T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782849 | |||||||
| chr11:75782866 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.122-1752G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782866 | |||||||
| chr11:75782937 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.122-1681G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75782937 | |||||||
| chr11:75783021 | G | A | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-1597G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783021 | |||||||
| chr11:75783165 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.122-1453A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783165 | |||||||
| chr11:75783178 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.122-1440G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783178 | |||||||
| chr11:75783283 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.122-1335G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783283 | |||||||
| chr11:75783581 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.122-1037A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783581 | |||||||
| chr11:75783582 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.122-1036G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783582 | |||||||
| chr11:75783768 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.122-850C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783768 | |||||||
| chr11:75783776 | T | C | 78 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(75): Show |
135 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.122-842T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783776 | |||||||
| chr11:75783968 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.122-650T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75783968 | |||||||
| chr11:75784181 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.122-437A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75784181 | |||||||
| chr11:75784377 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.122-241C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75784377 | |||||||
| chr11:75784475 | G | A | 8 | a0001c0001t0002g0007 a0001c0001t0002g0024 a0001c0001t0002g0049 others(5): Show |
12 | HG00438.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-143G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75784475 | |||||||
| chr11:75784531 | G | T | 1 | a0001c0003t0002g0012 | 3 | HG01884.hp1 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.122-87G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 1/7 | chr11 | 75784531 | |||||||
| chr11:75784857 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.250+111C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75784857 | |||||||
| chr11:75785199 | A | G | 1 | a0001c0001t0006g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.250+453A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785199 | |||||||
| chr11:75785348 | T | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.250+602T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785348 | |||||||
| chr11:75785410 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.250+664C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785410 | |||||||
| chr11:75785424 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.250+678G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785424 | |||||||
| chr11:75785649 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.250+903C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785649 | |||||||
| chr11:75785783 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.250+1037G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785783 | |||||||
| chr11:75785787 | A | G | 1 | a0001c0001t0005g0129 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.250+1041A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785787 | |||||||
| chr11:75785970 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.250+1224A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75785970 | |||||||
| chr11:75786024 | G | A | 1 | a0005c0010t0001g0115 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.250+1278G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786024 | |||||||
| chr11:75786186 | TAA | T | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+1442_250+1443d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75786186 | ||||||
| chr11:75786246 | A | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0101 a0001c0001t0001g0102 |
5 | HG01123.hp2 HG01192.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+1500A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786246 | |||||||
| chr11:75786323 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.250+1577T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786323 | |||||||
| chr11:75786398 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.250+1652A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786398 | |||||||
| chr11:75786749 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.250+2003C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786749 | |||||||
| chr11:75786948 | C | A | 1 | a0001c0003t0002g0067 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.250+2202C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75786948 | |||||||
| chr11:75787076 | GAT | G | 23 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(20): Show |
66 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.250+2333_250+2334d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75787076 | ||||||
| chr11:75787189 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.250+2443A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787189 | |||||||
| chr11:75787195 | A | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(28): Show |
75 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.250+2449A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787195 | |||||||
| chr11:75787218 | AT | A | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.250+2473delT | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787218 | |||||||
| chr11:75787386 | C | A | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+2640C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787386 | |||||||
| chr11:75787393 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0107 a0001c0001t0001g0128 |
4 | HG00597.hp2 HG00621.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+2647C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787393 | |||||||
| chr11:75787486 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0157 |
6 | NA18953.hp2 NA18954.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2702A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787486 | |||||||
| chr11:75787489 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.251-2699G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787489 | |||||||
| chr11:75787596 | A | T | 8 | a0001c0003t0002g0011 a0002c0002t0002g0063 a0002c0002t0003g0026 others(5): Show |
12 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.251-2592A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787596 | |||||||
| chr11:75787867 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0116 |
3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.251-2321G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787867 | |||||||
| chr11:75787968 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.251-2220G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787968 | |||||||
| chr11:75787969 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.251-2219C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75787969 | |||||||
| chr11:75788192 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.251-1996T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788192 | |||||||
| chr11:75788332 | G | A | 2 | a0001c0001t0001g0112 a0001c0005t0001g0016 |
4 | HG00621.hp2 HG02129.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-1856G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788332 | |||||||
| chr11:75788407 | T | C | 31 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(28): Show |
75 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.251-1781T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788407 | |||||||
| chr11:75788626 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.251-1562A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788626 | |||||||
| chr11:75788677 | A | C | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.251-1511A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788677 | |||||||
| chr11:75788839 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0086 |
2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.251-1349A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75788839 | |||||||
| chr11:75788970 | AAG | A | 3 | a0001c0001t0002g0056 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.251-1212_251-1211d others(4): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75788970 | ||||||
| chr11:75789091 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.251-1097A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789091 | |||||||
| chr11:75789117 | C | T | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.251-1071C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789117 | |||||||
| chr11:75789148 | G | GT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0102 a0001c0001t0001g0123 others(3): Show |
9 | HG01192.hp2 HG02132.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-1027dupT | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75789148 | ||||||
| chr11:75789211 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0132 |
3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.251-977G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789211 | |||||||
| chr11:75789467 | C | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0086 |
2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.251-721C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789467 | |||||||
| chr11:75789521 | T | C | 7 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-667T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789521 | |||||||
| chr11:75789568 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18989.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.251-620G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789568 | |||||||
| chr11:75789757 | A | C | 1 | a0001c0001t0001g0053 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.251-431A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789757 | |||||||
| chr11:75789792 | CAG | C | 8 | a0001c0001t0002g0007 a0001c0001t0002g0024 a0001c0001t0002g0049 others(5): Show |
12 | HG00438.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-393_251-392del others(2): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 75789792 | ||||||
| chr11:75789975 | C | T | 7 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-213C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75789975 | |||||||
| chr11:75790002 | G | T | 1 | a0001c0001t0002g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.251-186G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75790002 | |||||||
| chr11:75790026 | G | A | 1 | a0002c0002t0003g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.251-162G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75790026 | |||||||
| chr11:75790034 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0082 others(1): Show |
6 | HG02622.hp1 HG02895.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-154A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75790034 | |||||||
| chr11:75790162 | C | G | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.251-26C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 2/7 | chr11 | 75790162 | |||||||
| chr11:75790429 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.358+134G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 3/7 | chr11 | 75790429 | |||||||
| chr11:75790429 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.358+134G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 3/7 | chr11 | 75790429 | |||||||
| chr11:75790807 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(176): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.429+76A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75790807 | |||||||
| chr11:75790829 | T | C | 5 | a0002c0002t0003g0026 a0002c0002t0003g0027 a0002c0002t0003g0059 others(2): Show |
7 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+98T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75790829 | |||||||
| chr11:75791092 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.429+361G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791092 | |||||||
| chr11:75791137 | C | G | 7 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+406C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791137 | |||||||
| chr11:75791147 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.429+416C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791147 | |||||||
| chr11:75791173 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.429+442G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791173 | |||||||
| chr11:75791196 | C | A | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.429+465C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791196 | |||||||
| chr11:75791216 | G | A | 12 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(9): Show |
12 | HG01243.hp1 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+485G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791216 | |||||||
| chr11:75791414 | G | A | 5 | a0002c0002t0003g0026 a0002c0002t0003g0027 a0002c0002t0003g0059 others(2): Show |
7 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+683G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791414 | |||||||
| chr11:75791487 | G | T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.429+756G>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791487 | |||||||
| chr11:75791673 | A | G | 4 | a0001c0003t0002g0011 a0001c0003t0002g0012 a0001c0003t0002g0067 others(1): Show |
8 | HG01074.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+942A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75791673 | |||||||
| chr11:75792181 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+1450C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792181 | |||||||
| chr11:75792272 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.429+1541C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792272 | |||||||
| chr11:75792379 | G | A | 9 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(6): Show |
9 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+1648G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792379 | |||||||
| chr11:75792468 | A | G | 2 | a0001c0001t0002g0013 a0002c0002t0003g0059 |
4 | HG02622.hp2 NA18986.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1737A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792468 | |||||||
| chr11:75792518 | C | T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.429+1787C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792518 | |||||||
| chr11:75792544 | C | T | 1 | a0001c0001t0006g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+1813C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792544 | |||||||
| chr11:75792595 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.429+1864G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792595 | |||||||
| chr11:75792601 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.429+1870A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792601 | |||||||
| chr11:75792710 | G | A | 6 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+1979G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792710 | |||||||
| chr11:75792711 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.429+1980C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792711 | |||||||
| chr11:75792765 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.429+2034A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792765 | |||||||
| chr11:75792915 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.429+2184C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792915 | |||||||
| chr11:75792922 | T | C | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+2191T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75792922 | |||||||
| chr11:75793047 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.429+2316C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793047 | |||||||
| chr11:75793124 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0055 |
3 | HG02280.hp2 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.429+2393G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793124 | |||||||
| chr11:75793136 | C | T | 9 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(6): Show |
9 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+2405C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793136 | |||||||
| chr11:75793265 | G | C | 6 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+2534G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793265 | |||||||
| chr11:75793614 | C | T | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.430-2714C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793614 | |||||||
| chr11:75793724 | A | C | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.430-2604A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75793724 | |||||||
| chr11:75793919 | TA | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(54): Show |
107 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.430-2407delA | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 75793919 | ||||||
| chr11:75794166 | G | A | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-2162G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794166 | |||||||
| chr11:75794239 | C | G | 4 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-2089C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794239 | |||||||
| chr11:75794782 | T | C | 36 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
84 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.430-1546T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794782 | |||||||
| chr11:75794905 | C | T | 16 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-1423C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794905 | |||||||
| chr11:75794938 | TCCCC | T | 5 | a0001c0001t0002g0056 a0001c0001t0002g0058 a0001c0001t0002g0085 others(2): Show |
5 | HG02109.hp1 HG02257.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-1388_430-1385d others(6): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 75794938 | ||||||
| chr11:75794942 | C | CT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(167): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.430-1386_430-1385i others(3): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794942 | |||||||
| chr11:75794942 | C | CTCCCCT | 9 | a0001c0001t0002g0005 a0001c0001t0002g0043 a0001c0001t0002g0044 others(6): Show |
13 | HG01243.hp1 HG02071.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.430-1386_430-1385i others(8): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794942 | |||||||
| chr11:75794942 | C | CTCTCCTC others(14): Show |
1 | a0001c0001t0001g0001 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.430-1386_430-1385i others(23): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794942 | |||||||
| chr11:75794944 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.430-1384T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794944 | |||||||
| chr11:75794949 | C | T | 1 | a0001c0001t0013g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.430-1379C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794949 | |||||||
| chr11:75794966 | C | T | 7 | a0002c0002t0002g0063 a0002c0002t0003g0026 a0002c0002t0003g0027 others(4): Show |
9 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-1362C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794966 | |||||||
| chr11:75794969 | C | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(35): Show |
68 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.430-1359C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794969 | |||||||
| chr11:75794978 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430-1350G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75794978 | |||||||
| chr11:75795130 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430-1198T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795130 | |||||||
| chr11:75795342 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-986A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795342 | |||||||
| chr11:75795390 | C | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
6 | NA18943.hp1 NA18951.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-938C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795390 | |||||||
| chr11:75795419 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.430-909C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795419 | |||||||
| chr11:75795476 | A | G | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.430-852A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795476 | |||||||
| chr11:75795540 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.430-788A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795540 | |||||||
| chr11:75795692 | A | G | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.430-636A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795692 | |||||||
| chr11:75795704 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0160 |
3 | HG01074.hp2 HG01256.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.430-624G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795704 | |||||||
| chr11:75795940 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0116 |
3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.430-388C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75795940 | |||||||
| chr11:75796044 | A | C | 1 | a0001c0003t0002g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.430-284A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75796044 | |||||||
| chr11:75796078 | A | G | 4 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-250A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75796078 | |||||||
| chr11:75796189 | A | C | 60 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
110 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.430-139A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75796189 | |||||||
| chr11:75796251 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.430-77A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 4/7 | chr11 | 75796251 | |||||||
| chr11:75796712 | T | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
6 | NA18943.hp1 NA18951.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+180T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 5/7 | chr11 | 75796712 | |||||||
| chr11:75796807 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0082 a0001c0001t0001g0083 |
4 | HG02895.hp2 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+275T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 5/7 | chr11 | 75796807 | |||||||
| chr11:75797112 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.635-46T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 5/7 | chr11 | 75797112 | |||||||
| chr11:75797692 | C | G | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.809+360C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797692 | |||||||
| chr11:75797737 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.809+405C>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797737 | |||||||
| chr11:75797743 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.809+411G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797743 | |||||||
| chr11:75797848 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.810-379C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797848 | |||||||
| chr11:75797941 | G | C | 12 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(9): Show |
12 | HG01243.hp1 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.810-286G>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75797941 | |||||||
| chr11:75798102 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.810-125C>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75798102 | |||||||
| chr11:75798172 | A | G | 4 | a0002c0002t0003g0026 a0002c0002t0003g0059 a0002c0002t0003g0061 others(1): Show |
5 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.810-55A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75798172 | |||||||
| chr11:75798173 | T | G | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.810-54T>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 6/7 | chr11 | 75798173 | |||||||
| chr11:75798451 | C | T | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1012+22C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798451 | |||||||
| chr11:75798591 | GGTA | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(28): Show |
75 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1012+170_1012+172d others(5): Show |
DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 75798591 | ||||||
| chr11:75798750 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1012+321A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798750 | |||||||
| chr11:75798768 | T | C | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG02055.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1012+339T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798768 | |||||||
| chr11:75798805 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0155 others(2): Show |
8 | HG01169.hp2 HG01243.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+376A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798805 | |||||||
| chr11:75798935 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1012+506G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75798935 | |||||||
| chr11:75799170 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1012+741T>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799170 | |||||||
| chr11:75799436 | A | G | 1 | a0001c0008t0010g0143 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1013-918A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799436 | |||||||
| chr11:75799540 | G | A | 4 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0174 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-814G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799540 | |||||||
| chr11:75799585 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1013-769C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799585 | |||||||
| chr11:75799611 | A | T | 4 | a0001c0003t0002g0011 a0001c0003t0002g0012 a0001c0003t0002g0067 others(1): Show |
8 | HG01074.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1013-743A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799611 | |||||||
| chr11:75799616 | T | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0099 others(6): Show |
11 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1013-738T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799616 | |||||||
| chr11:75799617 | T | A | 3 | a0001c0001t0002g0056 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG02257.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1013-737T>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799617 | |||||||
| chr11:75799626 | A | T | 2 | a0001c0003t0002g0011 a0001c0003t0002g0012 |
6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-728A>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799626 | |||||||
| chr11:75799717 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1013-637G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799717 | |||||||
| chr11:75799758 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1013-596C>T | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799758 | |||||||
| chr11:75799994 | A | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0145 a0001c0001t0001g0148 others(2): Show |
7 | HG00544.hp2 NA18962.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1013-360A>C | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75799994 | |||||||
| chr11:75800276 | G | A | 2 | a0001c0001t0002g0056 a0001c0001t0002g0086 |
2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1013-78G>A | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75800276 | |||||||
| chr11:75800291 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0159 |
2 | HG01169.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1013-63A>G | DGAT2 | ENSG00000062282.15 | transcript | ENST00000228027.12 | protein_coding | 7/7 | chr11 | 75800291 |