Search by Gene
| Item | Value |
|---|---|
| geneid | 39 |
| ensemblid | ENSG00000120437.9 |
| hgncid | 94 |
| symbol | ACAT2 |
| name | acetyl-CoA acetyltransferase 2 |
| refseq_nuc | NM_005891.3 |
| refseq_prot | NP_005882.2 |
| ensembl_nuc | ENST00000367048.5 |
| ensembl_prot | ENSP00000356015.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 159762045 |
| end | 159779112 |
| strand | + |
| ver | v1.2 |
| region | chr6:159762045-159779112 |
| region5000 | chr6:159757045-159784112 |
| regionname0 | ACAT2_chr6_159762045_159779112 |
| regionname5000 | ACAT2_chr6_159757045_159784112 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 397 | 263 | 63 | 31 | 137 | 6 | 25 | ACAT2_chr6_159757045_159784112 | ACAT2 | MNAGS others(392): Show |
chr6 | 159757045 | 159784112 |
| a0002 | 0/1 | 397 | 139 | 27 | 47 | 35 | 8 | 21 | ACAT2_chr6_159757045_159784112 | ACAT2 | MNAGS others(392): Show |
chr6 | 159757045 | 159784112 |
| a0003 | 0/0 | 397 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | MNAGS others(392): Show |
chr6 | 159757045 | 159784112 |
| a0004 | 0/0 | 397 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | MNAGS others(392): Show |
chr6 | 159757045 | 159784112 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1191 | 134 | 41 | 13 | 65 | 3 | 11 | ACAT2_chr6_159757045_159784112 | ACAT2 | ATGAA others(1186): Show |
chr6 | 159757045 | 159784112 | ||
| a0001c0002 | 0/0 | 1191 | 121 | 14 | 18 | 72 | 3 | 14 | ACAT2_chr6_159757045_159784112 | ACAT2 | ATGAA others(1186): Show |
chr6 | 159757045 | 159784112 | ||
| a0001c0005 | 0/0 | 1191 | 8 | 8 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | ATGAA others(1186): Show |
chr6 | 159757045 | 159784112 | ||
| a0002c0003 | 0/1 | 1191 | 88 | 23 | 25 | 23 | 5 | 11 | ACAT2_chr6_159757045_159784112 | ACAT2 | ATGAA others(1186): Show |
chr6 | 159757045 | 159784112 | ||
| a0002c0004 | 0/0 | 1191 | 51 | 4 | 22 | 12 | 3 | 10 | ACAT2_chr6_159757045_159784112 | ACAT2 | ATGAA others(1186): Show |
chr6 | 159757045 | 159784112 | ||
| a0003c0006 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | ATGAA others(1186): Show |
chr6 | 159757045 | 159784112 | ||
| a0004c0007 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | ATGAA others(1186): Show |
chr6 | 159757045 | 159784112 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1520 | 133 | 41 | 13 | 64 | 3 | 11 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0001c0001t0005 | 0/0 | 1520 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0001c0002t0002 | 0/0 | 1520 | 120 | 14 | 18 | 71 | 3 | 14 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0001c0002t0004 | 0/0 | 1520 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0001c0005t0001 | 0/0 | 1520 | 8 | 8 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0002c0003t0001 | 0/1 | 1520 | 88 | 23 | 25 | 23 | 5 | 11 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0002c0004t0001 | 0/0 | 1520 | 47 | 4 | 22 | 12 | 3 | 6 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0002c0004t0002 | 0/0 | 1520 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0002c0004t0003 | 0/0 | 1520 | 3 | 0 | 0 | 0 | 0 | 3 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0003c0006t0001 | 0/0 | 1520 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| a0004c0007t0002 | 0/0 | 1520 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | AGCTT others(1515): Show |
chr6 | 159757045 | 159784112 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 40 | 1 | 2 | 29 | 2 | 5 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0004 | 0/0 | 18 | 6 | 2 | 10 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0001 | 0/0 | 57 | 8 | 4 | 40 | 2 | 3 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0005 | 0/0 | 11 | 0 | 1 | 9 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0006 | 0/0 | 9 | 0 | 2 | 4 | 0 | 3 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0011 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0019 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0031 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0005t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0001c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0003 | 0/0 | 27 | 5 | 9 | 6 | 3 | 4 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0010 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0013 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0014 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0007 | 0/0 | 8 | 0 | 4 | 3 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0015 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0022 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0023 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0002c0004t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0003c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| a0004c0007t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0041 | EUR | GBR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00099 | hp2 | a0002 | c0004 | t0001 | g0133 | EUR | GBR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0097 | EUR | GBR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00140 | hp2 | a0002 | c0004 | t0001 | g0024 | EUR | GBR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | FIN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00280 | hp2 | a0002 | c0004 | t0001 | g0023 | EUR | FIN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0030 | EUR | FIN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00558 | hp1 | a0002 | c0004 | t0001 | g0131 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0010 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00639 | hp2 | a0002 | c0004 | t0001 | g0114 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00733 | hp2 | a0002 | c0004 | t0001 | g0130 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00735 | hp1 | a0002 | c0004 | t0001 | g0015 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00735 | hp2 | a0002 | c0004 | t0001 | g0134 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00738 | hp1 | a0002 | c0004 | t0001 | g0126 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0010 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0029 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01081 | hp1 | a0002 | c0004 | t0001 | g0038 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01099 | hp2 | a0002 | c0004 | t0001 | g0007 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0015 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01192 | hp2 | a0002 | c0004 | t0001 | g0023 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01255 | hp1 | a0002 | c0004 | t0001 | g0135 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01255 | hp2 | a0002 | c0004 | t0001 | g0007 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0115 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0024 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0105 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0041 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01361 | hp2 | a0002 | c0003 | t0001 | g0010 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01496 | hp1 | a0002 | c0004 | t0001 | g0024 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01515 | hp1 | a0002 | c0003 | t0001 | g0003 | EUR | IBS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01884 | hp1 | a0002 | c0004 | t0001 | g0132 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01928 | hp1 | a0002 | c0004 | t0001 | g0007 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01934 | hp1 | a0002 | c0004 | t0001 | g0015 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01943 | hp1 | a0002 | c0004 | t0001 | g0123 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0014 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0010 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01978 | hp2 | a0002 | c0004 | t0001 | g0007 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0014 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01993 | hp2 | a0002 | c0004 | t0001 | g0036 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0013 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02056 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | KHV | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0081 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02148 | hp1 | a0002 | c0003 | t0001 | g0109 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02148 | hp2 | a0002 | c0004 | t0001 | g0137 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CDX | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02165 | hp2 | a0002 | c0004 | t0001 | g0022 | EAS | CDX | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0102 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0010 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0010 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02273 | hp2 | a0002 | c0004 | t0001 | g0125 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0008 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0037 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0036 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02300 | hp1 | a0002 | c0004 | t0001 | g0022 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02300 | hp2 | a0002 | c0003 | t0001 | g0037 | AMR | PEL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02809 | hp2 | a0002 | c0004 | t0001 | g0039 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02818 | hp2 | a0002 | c0003 | t0001 | g0104 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0058 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02896 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03490 | hp1 | a0002 | c0004 | t0001 | g0127 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03490 | hp2 | a0002 | c0003 | t0001 | g0116 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0101 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0003 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0003 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0107 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0110 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | GWD | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03654 | hp2 | a0002 | c0004 | t0002 | g0061 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03669 | hp1 | a0002 | c0003 | t0001 | g0003 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03704 | hp1 | a0002 | c0004 | t0001 | g0038 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03831 | hp2 | a0002 | c0004 | t0003 | g0100 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03834 | hp1 | a0002 | c0004 | t0001 | g0007 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03927 | hp1 | a0002 | c0004 | t0001 | g0015 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03942 | hp1 | a0002 | c0004 | t0003 | g0124 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0068 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0094 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04184 | hp2 | a0002 | c0004 | t0001 | g0023 | SAS | BEB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04199 | hp1 | a0002 | c0004 | t0003 | g0015 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0098 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0028 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0112 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0095 | SAS | STU | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18906 | hp2 | a0002 | c0004 | t0001 | g0039 | AFR | YRI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18949 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18949 | hp2 | a0002 | c0004 | t0001 | g0122 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18967 | hp1 | a0002 | c0004 | t0001 | g0136 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18972 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18977 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18978 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0120 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18985 | hp2 | a0003 | c0006 | t0001 | g0148 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18986 | hp1 | a0004 | c0007 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18987 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18991 | hp2 | a0002 | c0004 | t0001 | g0022 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18992 | hp1 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0062 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18997 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19012 | hp1 | a0002 | c0004 | t0001 | g0040 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | LWK | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0118 | AFR | LWK | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19054 | hp2 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0108 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19063 | hp1 | a0002 | c0003 | t0001 | g0119 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19065 | hp1 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19074 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19077 | hp1 | a0002 | c0004 | t0001 | g0022 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19078 | hp2 | a0002 | c0004 | t0001 | g0129 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19083 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19090 | hp2 | a0002 | c0004 | t0001 | g0040 | EAS | JPT | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0008 | AFR | YRI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0003 | EUR | TSI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20805 | hp2 | a0002 | c0003 | t0001 | g0003 | EUR | TSI | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20905 | hp1 | a0002 | c0004 | t0001 | g0128 | SAS | GIH | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0003 | SAS | GIH | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0106 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | CLM | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0003 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0003 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG02559 | hp2 | a0002 | c0003 | t0001 | g0096 | AFR | ACB | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0003 | AFR | MSL | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0113 | AFR | USA | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20300 | hp1 | a0002 | c0004 | t0001 | g0023 | AFR | USA | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | USA | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0099 | REF | REF | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | ACAT2_chr6_159757045_159784112 | ACAT2 | chr6 | 159757045 | 159784112 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159775311 | A | G | 1 | a0002 | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
missense_variant&splice_region_variant | MODERATE | c.632A>G | p.Lys211Arg | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/9 | 675/1520 | 632/1194 | 211/397 | chr6 | 159775311 | |||
| chr6:159777395 | C | G | 1 | a0004 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.851C>G | p.Ser284Cys | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/9 | 894/1520 | 851/1194 | 284/397 | chr6 | 159777395 | |||
| chr6:159778225 | C | G | 1 | a0003 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.968C>G | p.Ala323Gly | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/9 | 1011/1520 | 968/1194 | 323/397 | chr6 | 159778225 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159775264 | T | G | 1 | a0001c0005 | 8 | HG02145.hp2 HG02809.hp1 HG02886.hp2 others(5): Show |
synonymous_variant | LOW | c.585T>G | p.Ala195Ala | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/9 | 628/1520 | 585/1194 | 195/397 | chr6 | 159775264 | |||
| chr6:159777327 | C | T | 2 | a0001c0002a0004c0007 | 122 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(119): Show |
synonymous_variant | LOW | c.783C>T | p.Val261Val | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/9 | 826/1520 | 783/1194 | 261/397 | chr6 | 159777327 | |||
| chr6:159777363 | G | A | 1 | a0002c0003 | 87 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(84): Show |
synonymous_variant | LOW | c.819G>A | p.Gly273Gly | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/9 | 862/1520 | 819/1194 | 273/397 | chr6 | 159777363 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159762051 | C | A | 1 | a0001c0002t0004 | 1 | NA18994.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37C>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/9 | 37 | chr6 | 159762051 | ||||||
| chr6:159762073 | G | A | 1 | a0002c0004t0003 | 3 | HG03831.hp2 HG03942.hp1 HG04199.hp1 |
5_prime_UTR_variant | MODIFIER | c.-15G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/9 | 15 | chr6 | 159762073 | ||||||
| chr6:159778942 | A | G | 1 | a0001c0001t0005 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 9/9 | 113 | chr6 | 159778942 | ||||||
| chr6:159778994 | A | C | 4 | a0001c0002t0002a0001c0002t0004a0002c0004t0002others(1): Show | 123 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*165A>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 9/9 | 165 | chr6 | 159778994 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159762293 | G | C | 126 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(123): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.55+151G>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/8 | chr6 | 159762293 | |||||||
| chr6:159762350 | C | T | 63 | a0002c0003t0001g0003a0002c0003t0001g0008a0002c0003t0001g0010others(60): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.55+208C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/8 | chr6 | 159762350 | |||||||
| chr6:159762383 | G | A | 1 | a0001c0002t0002g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.55+241G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/8 | chr6 | 159762383 | |||||||
| chr6:159762413 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.55+271A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/8 | chr6 | 159762413 | |||||||
| chr6:159762491 | G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 10 | HG02615.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.55+349G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/8 | chr6 | 159762491 | |||||||
| chr6:159762581 | T | G | 1 | a0001c0002t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.56-338T>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/8 | chr6 | 159762581 | |||||||
| chr6:159762584 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.56-335G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/8 | chr6 | 159762584 | |||||||
| chr6:159762617 | G | C | 2 | a0002c0003t0001g0094a0002c0003t0001g0095 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.56-302G>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 1/8 | chr6 | 159762617 | |||||||
| chr6:159763124 | A | T | 19 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(16): Show | 31 | HG00323.hp2 HG01109.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.190+71A>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763124 | |||||||
| chr6:159763455 | G | T | 1 | a0002c0004t0001g0137 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.190+402G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763455 | |||||||
| chr6:159763543 | A | G | 1 | a0001c0002t0002g0085 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.190+490A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763543 | |||||||
| chr6:159763568 | A | G | 1 | a0002c0003t0001g0041 | 2 | HG00099.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.190+515A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763568 | |||||||
| chr6:159763629 | C | CT | 21 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0027others(18): Show | 62 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.190+604dupT | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | C | CTT | 8 | a0001c0001t0001g0047a0001c0001t0001g0080a0001c0001t0001g0082others(5): Show | 10 | HG00621.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.190+603_190+604dup others(2): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | C | CTTT | 5 | a0001c0001t0001g0084a0002c0003t0001g0037a0002c0004t0001g0036others(2): Show | 7 | HG00738.hp1 HG01069.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+602_190+604dup others(3): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | C | CTTTT | 13 | a0001c0001t0001g0051a0002c0004t0001g0007a0002c0004t0001g0015others(10): Show | 28 | HG00099.hp2 HG00558.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.190+601_190+604dup others(4): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | C | CTTTTT | 9 | a0001c0001t0001g0052a0001c0001t0001g0054a0002c0004t0001g0023others(6): Show | 15 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.190+600_190+604dup others(5): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.190+584_190+585ins others(14): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0053 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190+595_190+604dup others(10): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | CT | C | 18 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0086others(15): Show | 33 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.190+604delT | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | CTT | C | 22 | a0002c0003t0001g0003a0002c0003t0001g0008a0002c0003t0001g0013others(19): Show | 63 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.190+603_190+604del others(2): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763629 | CTTTTTTT | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0020 | 9 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.190+598_190+604del others(7): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159763629 | ||||||
| chr6:159763646 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.190+593T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763646 | |||||||
| chr6:159763690 | A | G | 35 | a0001c0002t0002g0001a0001c0002t0002g0005a0001c0002t0002g0006others(32): Show | 123 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.190+637A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763690 | |||||||
| chr6:159763701 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.190+648G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763701 | |||||||
| chr6:159763727 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.190+674T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763727 | |||||||
| chr6:159763858 | C | T | 124 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(121): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.190+805C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763858 | |||||||
| chr6:159763918 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.190+865G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159763918 | |||||||
| chr6:159764033 | G | A | 1 | a0002c0003t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.190+980G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764033 | |||||||
| chr6:159764071 | A | G | 1 | a0002c0003t0001g0034 | 2 | NA18992.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.190+1018A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764071 | |||||||
| chr6:159764119 | A | C | 5 | a0001c0002t0002g0019a0001c0002t0002g0072a0001c0002t0002g0073others(2): Show | 8 | HG01123.hp2 HG01192.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.190+1066A>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764119 | |||||||
| chr6:159764125 | C | T | 1 | a0002c0003t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.190+1072C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764125 | |||||||
| chr6:159764296 | A | T | 1 | a0002c0004t0001g0133 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.190+1243A>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764296 | |||||||
| chr6:159764345 | G | A | 65 | a0001c0001t0001g0056a0001c0001t0001g0084a0002c0003t0001g0003others(62): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.190+1292G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764345 | |||||||
| chr6:159764448 | A | ATTG | 5 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+1397_190+1398i others(5): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159764448 | ||||||
| chr6:159764558 | C | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.190+1505C>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764558 | |||||||
| chr6:159764630 | A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 10 | HG02615.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.190+1577A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764630 | |||||||
| chr6:159764658 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.190+1605G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764658 | |||||||
| chr6:159764700 | T | C | 1 | a0001c0002t0002g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190+1647T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159764700 | |||||||
| chr6:159765105 | G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0084 | 2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.191-1900G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765105 | |||||||
| chr6:159765127 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191-1878T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765127 | |||||||
| chr6:159765180 | A | G | 1 | a0001c0002t0002g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.191-1825A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765180 | |||||||
| chr6:159765361 | C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0045a0001c0001t0001g0143 | 6 | NA18959.hp2 NA18968.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-1644C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765361 | |||||||
| chr6:159765440 | T | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0005t0001g0009others(2): Show | 10 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.191-1565T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765440 | |||||||
| chr6:159765500 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.191-1505C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765500 | |||||||
| chr6:159765614 | G | C | 65 | a0001c0001t0001g0056a0001c0001t0001g0084a0002c0003t0001g0003others(62): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.191-1391G>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765614 | |||||||
| chr6:159765619 | G | A | 65 | a0001c0001t0001g0056a0001c0001t0001g0084a0002c0003t0001g0003others(62): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.191-1386G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765619 | |||||||
| chr6:159765679 | CCCT | C | 108 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0033others(105): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.191-1323_191-1321d others(5): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159765679 | ||||||
| chr6:159765680 | CCT | C | 13 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0089others(10): Show | 21 | HG00323.hp2 HG00735.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.191-1323_191-1322d others(4): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159765680 | ||||||
| chr6:159765681 | CT | C | 2 | a0001c0001t0001g0012a0002c0004t0001g0015 | 3 | HG01169.hp1 HG01169.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.191-1323delT | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765681 | |||||||
| chr6:159765682 | T | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0054 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.191-1323T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765682 | |||||||
| chr6:159765682 | T | G | 1 | a0001c0002t0002g0070 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.191-1323T>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765682 | |||||||
| chr6:159765683 | C | G | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191-1322C>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765683 | |||||||
| chr6:159765683 | C | T | 6 | a0002c0003t0001g0021a0002c0003t0001g0034a0002c0003t0001g0035others(3): Show | 11 | HG02056.hp2 NA18974.hp2 NA18978.hp1 others(8): Show |
intron_variant | MODIFIER | c.191-1322C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765683 | |||||||
| chr6:159765685 | C | G | 40 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0002t0002g0001others(37): Show | 134 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.191-1320C>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765685 | |||||||
| chr6:159765723 | A | G | 1 | a0001c0001t0001g0045 | 2 | NA19062.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.191-1282A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765723 | |||||||
| chr6:159765787 | G | C | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191-1218G>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765787 | |||||||
| chr6:159765840 | T | C | 42 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(39): Show | 136 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.191-1165T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765840 | |||||||
| chr6:159765888 | A | C | 63 | a0002c0003t0001g0003a0002c0003t0001g0008a0002c0003t0001g0010others(60): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.191-1117A>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765888 | |||||||
| chr6:159765980 | T | C | 3 | a0002c0003t0001g0008a0002c0003t0001g0113a0002c0003t0001g0121 | 9 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.191-1025T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159765980 | |||||||
| chr6:159766190 | A | G | 5 | a0001c0002t0002g0030a0001c0002t0002g0068a0001c0002t0002g0069others(2): Show | 6 | HG00323.hp1 HG01070.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-815A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159766190 | |||||||
| chr6:159766251 | G | A | 1 | a0002c0003t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.191-754G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159766251 | |||||||
| chr6:159766265 | G | A | 1 | a0002c0004t0001g0128 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.191-740G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159766265 | |||||||
| chr6:159766379 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191-626T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159766379 | |||||||
| chr6:159766395 | A | AC | 37 | a0001c0001t0001g0089a0001c0002t0002g0001a0001c0002t0002g0005others(34): Show | 124 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.191-603dupC | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159766395 | ||||||
| chr6:159766406 | C | CT | 8 | a0001c0001t0001g0033a0001c0002t0002g0066a0001c0002t0002g0067others(5): Show | 17 | HG01168.hp1 HG01891.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.191-587dupT | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159766406 | ||||||
| chr6:159766465 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.191-540G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159766465 | |||||||
| chr6:159766833 | CTG | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 10 | HG02615.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.191-169_191-168del others(2): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 159766833 | ||||||
| chr6:159766945 | C | T | 1 | a0002c0003t0001g0119 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.191-60C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 2/8 | chr6 | 159766945 | |||||||
| chr6:159767315 | A | G | 1 | a0002c0004t0001g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.372+129A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 3/8 | chr6 | 159767315 | |||||||
| chr6:159767504 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.372+318T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 3/8 | chr6 | 159767504 | |||||||
| chr6:159767859 | T | C | 109 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(106): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.373-652T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 3/8 | chr6 | 159767859 | |||||||
| chr6:159767975 | C | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.373-536C>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 3/8 | chr6 | 159767975 | |||||||
| chr6:159768310 | G | A | 1 | a0001c0002t0002g0066 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.373-201G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 3/8 | chr6 | 159768310 | |||||||
| chr6:159768347 | A | G | 1 | a0001c0001t0001g0046 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.373-164A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 3/8 | chr6 | 159768347 | |||||||
| chr6:159768387 | G | A | 1 | a0002c0003t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.373-124G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 3/8 | chr6 | 159768387 | |||||||
| chr6:159768459 | G | T | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.373-52G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 3/8 | chr6 | 159768459 | |||||||
| chr6:159768714 | T | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.490+86T>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159768714 | |||||||
| chr6:159769033 | T | TGGGGGGG others(95): Show |
1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+408_490+409ins others(102): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159769033 | ||||||
| chr6:159769036 | GAAATCAA others(76): Show |
G | 1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+409_490+491del others(83): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769036 | |||||||
| chr6:159769121 | A | G | 1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+493A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769121 | |||||||
| chr6:159769147 | A | G | 1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+519A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769147 | |||||||
| chr6:159769148 | T | TGGGGGGG others(40): Show |
1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+521_490+522ins others(47): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159769148 | ||||||
| chr6:159769149 | GCAGCAAT others(43): Show |
G | 1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+522_490+571del others(50): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769149 | |||||||
| chr6:159769204 | A | G | 1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+576A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769204 | |||||||
| chr6:159769205 | A | G | 1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+577A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769205 | |||||||
| chr6:159769206 | A | G | 1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+578A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769206 | |||||||
| chr6:159769207 | A | G | 1 | a0002c0003t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+579A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769207 | |||||||
| chr6:159769586 | A | T | 41 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(38): Show | 135 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.490+958A>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769586 | |||||||
| chr6:159769744 | T | C | 5 | a0001c0002t0002g0030a0001c0002t0002g0068a0001c0002t0002g0069others(2): Show | 6 | HG00323.hp1 HG01070.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+1116T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769744 | |||||||
| chr6:159769779 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.490+1151G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769779 | |||||||
| chr6:159769869 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.490+1241C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159769869 | |||||||
| chr6:159770205 | C | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0139 | 3 | HG02683.hp2 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.490+1577C>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159770205 | |||||||
| chr6:159770567 | C | T | 5 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+1939C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159770567 | |||||||
| chr6:159770626 | A | G | 1 | a0003c0006t0001g0148 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.490+1998A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159770626 | |||||||
| chr6:159770785 | C | CCAGGCAC others(46): Show |
1 | a0001c0002t0002g0065 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.490+2173_490+2174i others(55): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159770785 | ||||||
| chr6:159770792 | C | T | 1 | a0001c0002t0002g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490+2164C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159770792 | |||||||
| chr6:159770802 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490+2174C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159770802 | |||||||
| chr6:159771066 | A | AAAATTAA others(3): Show |
34 | a0001c0001t0001g0033a0001c0002t0002g0001a0001c0002t0002g0005others(31): Show | 122 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.490+2457_490+2466d others(12): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159771066 | ||||||
| chr6:159771066 | A | AAAATTAA others(8): Show |
4 | a0001c0002t0002g0028a0001c0005t0001g0009a0001c0005t0001g0058others(1): Show | 10 | HG01099.hp1 HG02145.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+2452_490+2466d others(17): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159771066 | ||||||
| chr6:159771066 | A | AAAATTAA others(13): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.490+2447_490+2466d others(22): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159771066 | ||||||
| chr6:159771116 | TCATGCCT others(126): Show |
T | 1 | a0001c0001t0001g0142 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.490+2507_490+2639d others(2): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159771116 | ||||||
| chr6:159771150 | T | C | 124 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(121): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.490+2522T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771150 | |||||||
| chr6:159771249 | G | A | 25 | a0001c0002t0002g0001a0001c0002t0002g0005a0001c0002t0002g0006others(22): Show | 106 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.490+2621G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771249 | |||||||
| chr6:159771311 | C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.490+2683C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771311 | |||||||
| chr6:159771336 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.490+2708C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771336 | |||||||
| chr6:159771360 | A | G | 1 | a0001c0002t0002g0030 | 2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.490+2732A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771360 | |||||||
| chr6:159771369 | A | G | 1 | a0001c0002t0002g0065 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.490+2741A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771369 | |||||||
| chr6:159771389 | A | T | 1 | a0001c0002t0002g0065 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.490+2761A>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771389 | |||||||
| chr6:159771650 | C | CA | 6 | a0001c0001t0001g0026a0001c0001t0001g0049a0001c0001t0001g0052others(3): Show | 8 | HG01109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+3036dupA | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159771650 | ||||||
| chr6:159771650 | CA | C | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0143others(4): Show | 12 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.490+3036delA | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 159771650 | ||||||
| chr6:159771733 | A | G | 5 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+3105A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771733 | |||||||
| chr6:159771896 | T | G | 124 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(121): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.490+3268T>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771896 | |||||||
| chr6:159771913 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.491-3257C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771913 | |||||||
| chr6:159771947 | C | T | 2 | a0002c0003t0001g0107a0002c0003t0001g0116 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.491-3223C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771947 | |||||||
| chr6:159771948 | G | A | 28 | a0002c0004t0001g0007a0002c0004t0001g0015a0002c0004t0001g0022others(25): Show | 49 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.491-3222G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771948 | |||||||
| chr6:159771951 | C | T | 1 | a0002c0003t0001g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.491-3219C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771951 | |||||||
| chr6:159771992 | G | A | 1 | a0001c0002t0002g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.491-3178G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159771992 | |||||||
| chr6:159772017 | A | C | 40 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(37): Show | 134 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.491-3153A>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772017 | |||||||
| chr6:159772041 | C | T | 1 | a0001c0002t0002g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.491-3129C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772041 | |||||||
| chr6:159772097 | T | C | 109 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(106): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.491-3073T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772097 | |||||||
| chr6:159772098 | G | A | 1 | a0001c0002t0002g0072 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.491-3072G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772098 | |||||||
| chr6:159772139 | T | C | 1 | a0002c0003t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.491-3031T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772139 | |||||||
| chr6:159772208 | C | A | 64 | a0002c0003t0001g0003a0002c0003t0001g0008a0002c0003t0001g0010others(61): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.491-2962C>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772208 | |||||||
| chr6:159772346 | A | T | 40 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(37): Show | 134 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.491-2824A>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772346 | |||||||
| chr6:159772393 | G | A | 2 | a0002c0004t0001g0130a0002c0004t0001g0134 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.491-2777G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772393 | |||||||
| chr6:159772399 | G | C | 1 | a0002c0003t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.491-2771G>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772399 | |||||||
| chr6:159772416 | A | T | 1 | a0001c0002t0002g0065 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.491-2754A>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772416 | |||||||
| chr6:159772433 | T | C | 124 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(121): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.491-2737T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772433 | |||||||
| chr6:159772502 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.491-2668T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772502 | |||||||
| chr6:159772580 | G | A | 124 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(121): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.491-2590G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772580 | |||||||
| chr6:159772600 | A | C | 1 | a0002c0003t0001g0010 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.491-2570A>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772600 | |||||||
| chr6:159772671 | G | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0084 | 2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.491-2499G>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772671 | |||||||
| chr6:159772682 | T | C | 64 | a0002c0003t0001g0003a0002c0003t0001g0008a0002c0003t0001g0010others(61): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.491-2488T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772682 | |||||||
| chr6:159772742 | A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0091 | 2 | HG01109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.491-2428A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772742 | |||||||
| chr6:159772821 | A | G | 109 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(106): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.491-2349A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772821 | |||||||
| chr6:159772846 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.491-2324G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772846 | |||||||
| chr6:159772885 | G | T | 122 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0033others(119): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.491-2285G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772885 | |||||||
| chr6:159772887 | G | T | 1 | a0001c0002t0002g0085 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.491-2283G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159772887 | |||||||
| chr6:159773187 | C | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0005t0001g0009others(2): Show | 10 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-1983C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773187 | |||||||
| chr6:159773328 | GACCTAGA others(28): Show |
G | 1 | a0001c0002t0002g0065 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.491-1841_491-1807d others(37): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773328 | |||||||
| chr6:159773366 | C | G | 1 | a0001c0002t0002g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.491-1804C>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773366 | |||||||
| chr6:159773406 | G | A | 1 | a0002c0003t0001g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.491-1764G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773406 | |||||||
| chr6:159773414 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.491-1756G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773414 | |||||||
| chr6:159773646 | G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 10 | HG02615.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.491-1524G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773646 | |||||||
| chr6:159773752 | G | A | 68 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(65): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.491-1418G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773752 | |||||||
| chr6:159773791 | A | G | 1 | a0001c0002t0002g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.491-1379A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773791 | |||||||
| chr6:159773850 | G | A | 124 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(121): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.491-1320G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773850 | |||||||
| chr6:159773936 | A | G | 1 | a0001c0002t0002g0076 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.491-1234A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159773936 | |||||||
| chr6:159774088 | G | A | 3 | a0002c0003t0001g0102a0002c0003t0001g0107a0002c0003t0001g0116 | 3 | HG02257.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.491-1082G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774088 | |||||||
| chr6:159774127 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.491-1043T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774127 | |||||||
| chr6:159774173 | G | C | 34 | a0001c0002t0002g0001a0001c0002t0002g0005a0001c0002t0002g0006others(31): Show | 122 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.491-997G>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774173 | |||||||
| chr6:159774482 | C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0086a0001c0001t0001g0088 | 4 | HG01884.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-688C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774482 | |||||||
| chr6:159774554 | C | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 10 | HG02615.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.491-616C>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774554 | |||||||
| chr6:159774646 | G | T | 1 | a0001c0001t0001g0045 | 2 | NA19062.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.491-524G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774646 | |||||||
| chr6:159774728 | G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0089 | 10 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.491-442G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774728 | |||||||
| chr6:159774734 | C | G | 3 | a0001c0005t0001g0009a0001c0005t0001g0058a0001c0005t0001g0081 | 8 | HG02145.hp2 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-436C>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774734 | |||||||
| chr6:159774867 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.491-303A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159774867 | |||||||
| chr6:159775142 | G | A | 1 | a0001c0002t0004g0062 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.491-28G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 4/8 | chr6 | 159775142 | |||||||
| chr6:159775319 | T | C | 1 | a0002c0003t0001g0103 | 1 | NA19070.hp1 | splice_region_variant&intron_variant | LOW | c.634+6T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775319 | |||||||
| chr6:159775431 | A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.634+118A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775431 | |||||||
| chr6:159775480 | A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02055.hp2 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.634+167A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775480 | |||||||
| chr6:159775528 | C | T | 1 | a0002c0003t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.634+215C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775528 | |||||||
| chr6:159775607 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.634+294A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775607 | |||||||
| chr6:159775742 | C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-408C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775742 | |||||||
| chr6:159775770 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.635-380G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775770 | |||||||
| chr6:159775770 | G | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-380G>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775770 | |||||||
| chr6:159775806 | C | T | 2 | a0001c0002t0002g0064a0001c0002t0002g0075 | 2 | NA18972.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.635-344C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 5/8 | chr6 | 159775806 | |||||||
| chr6:159776305 | C | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0084 | 2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.757+33C>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776305 | |||||||
| chr6:159776338 | TTC | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02055.hp2 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.757+70_757+71delCT | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 159776338 | ||||||
| chr6:159776544 | T | C | 64 | a0002c0003t0001g0003a0002c0003t0001g0008a0002c0003t0001g0010others(61): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.757+272T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776544 | |||||||
| chr6:159776743 | A | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.757+471A>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776743 | |||||||
| chr6:159776770 | C | T | 35 | a0002c0003t0001g0003a0002c0003t0001g0008a0002c0003t0001g0010others(32): Show | 87 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.757+498C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776770 | |||||||
| chr6:159776826 | T | C | 4 | a0002c0004t0001g0022a0002c0004t0001g0040a0002c0004t0001g0122others(1): Show | 8 | HG02165.hp2 HG02300.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.758-476T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776826 | |||||||
| chr6:159776852 | A | G | 40 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(37): Show | 134 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.758-450A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776852 | |||||||
| chr6:159776888 | A | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.758-414A>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776888 | |||||||
| chr6:159776911 | C | T | 2 | a0002c0003t0001g0105a0002c0003t0001g0115 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.758-391C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776911 | |||||||
| chr6:159776933 | C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(3): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.758-369C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159776933 | |||||||
| chr6:159777180 | T | C | 7 | a0002c0004t0001g0024a0002c0004t0001g0038a0002c0004t0001g0114others(4): Show | 10 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.758-122T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 6/8 | chr6 | 159777180 | |||||||
| chr6:159777698 | C | T | 1 | a0001c0002t0002g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.912+242C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | chr6 | 159777698 | |||||||
| chr6:159777742 | G | A | 5 | a0001c0002t0002g0030a0001c0002t0002g0068a0001c0002t0002g0069others(2): Show | 6 | HG00323.hp1 HG01070.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+286G>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | chr6 | 159777742 | |||||||
| chr6:159777744 | CTA | C | 69 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(66): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.912+290_912+291del others(2): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 159777744 | ||||||
| chr6:159777911 | C | T | 1 | a0002c0004t0001g0127 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.913-259C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | chr6 | 159777911 | |||||||
| chr6:159777912 | A | G | 69 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(66): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.913-258A>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | chr6 | 159777912 | |||||||
| chr6:159777936 | TTTTAAGA others(3): Show |
T | 1 | a0001c0001t0001g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.913-229_913-220del others(10): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 159777936 | ||||||
| chr6:159777980 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.913-190C>T | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | chr6 | 159777980 | |||||||
| chr6:159778052 | AC | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0005t0001g0009others(2): Show | 10 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.913-117delC | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | chr6 | 159778052 | |||||||
| chr6:159778113 | T | C | 1 | a0001c0002t0002g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.913-57T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 7/8 | chr6 | 159778113 | |||||||
| chr6:159778392 | TA | T | 40 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(37): Show | 134 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1023+113delA | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778392 | |||||||
| chr6:159778394 | C | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0084 | 2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1023+114C>G | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778394 | |||||||
| chr6:159778421 | GTT | G | 4 | a0001c0002t0002g0006a0001c0002t0002g0011a0001c0002t0002g0057others(1): Show | 16 | HG00597.hp1 HG01106.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1023+143_1023+144d others(4): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 159778421 | ||||||
| chr6:159778422 | TTTA | T | 31 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0002t0002g0001others(28): Show | 103 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1023+143_1023+145d others(5): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778422 | |||||||
| chr6:159778422 | TTTAA | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 7 | HG02055.hp2 HG02886.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.1023+143_1023+146d others(6): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778422 | |||||||
| chr6:159778422 | TTTAAAA | T | 4 | a0002c0003t0001g0008a0002c0004t0001g0038a0002c0004t0001g0040others(1): Show | 4 | HG00738.hp1 HG01081.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+143_1023+148d others(8): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778422 | |||||||
| chr6:159778422 | TTTAAAAA | T | 63 | a0002c0003t0001g0003a0002c0003t0001g0008a0002c0003t0001g0010others(60): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1023+143_1023+149d others(9): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778422 | |||||||
| chr6:159778422 | TTTAAAAA others(3): Show |
T | 1 | a0001c0002t0002g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1023+143_1023+152d others(12): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778422 | |||||||
| chr6:159778422 | TTTAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1023+143_1023+153d others(13): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778422 | |||||||
| chr6:159778422 | TTTAAAAA others(5): Show |
T | 3 | a0001c0005t0001g0009a0001c0005t0001g0058a0001c0005t0001g0081 | 8 | HG02145.hp2 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023+143_1023+154d others(14): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778422 | |||||||
| chr6:159778423 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1023+143T>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778423 | |||||||
| chr6:159778423 | T | TA | 4 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(1): Show | 6 | HG01168.hp2 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023+143_1023+144i others(3): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778423 | |||||||
| chr6:159778423 | T | TAA | 5 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0032others(2): Show | 7 | HG00323.hp2 HG01169.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+143_1023+144i others(4): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778423 | |||||||
| chr6:159778423 | TTAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1023+144_1023+153d others(12): Show |
ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778423 | |||||||
| chr6:159778424 | T | A | 13 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(10): Show | 25 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1023+144T>A | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778424 | |||||||
| chr6:159778424 | T | TA | 2 | a0001c0001t0001g0016a0001c0001t0001g0146 | 6 | HG01109.hp1 HG02080.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1023+169dupA | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 159778424 | ||||||
| chr6:159778424 | TA | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0141others(2): Show | 8 | HG00609.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+169delA | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 159778424 | ||||||
| chr6:159778474 | G | C | 6 | a0002c0003t0001g0008a0002c0003t0001g0104a0002c0003t0001g0110others(3): Show | 12 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1024-185G>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778474 | |||||||
| chr6:159778655 | T | C | 109 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0083others(106): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
splice_region_variant&intron_variant | LOW | c.1024-4T>C | ACAT2 | ENSG00000120437.9 | transcript | ENST00000367048.5 | protein_coding | 8/8 | chr6 | 159778655 |