Search by Gene
| Item | Value |
|---|---|
| geneid | 341392 |
| ensemblid | ENSG00000215009.6 |
| hgncid | 32016 |
| symbol | ACSM4 |
| name | acyl-CoA synthetase medium chain family member 4 |
| refseq_nuc | NM_001080454.2 |
| refseq_prot | NP_001073923.1 |
| ensembl_nuc | ENST00000399422.5 |
| ensembl_prot | ENSP00000382349.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 7304072 |
| end | 7328719 |
| strand | + |
| ver | v1.2 |
| region | chr12:7304072-7328719 |
| region5000 | chr12:7299072-7333719 |
| regionname0 | ACSM4_chr12_7304072_7328719 |
| regionname5000 | ACSM4_chr12_7299072_7333719 |
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 | 1/1 | 580 | 390 | 76 | 70 | 180 | 18 | 44 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| a0002 | 0/0 | 580 | 16 | 14 | 2 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| a0003 | 0/0 | 356 | 13 | 6 | 2 | 5 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(351): Show |
chr12 | 7299072 | 7333719 |
| a0004 | 0/0 | 580 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| a0005 | 0/0 | 580 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| a0006 | 0/0 | 580 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| a0007 | 0/0 | 580 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| a0008 | 0/0 | 580 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| a0009 | 0/0 | 580 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| a0010 | 0/0 | 580 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | MKIFF others(575): Show |
chr12 | 7299072 | 7333719 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1740 | 264 | 53 | 47 | 119 | 8 | 36 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0001c0002 | 0/1 | 1740 | 111 | 11 | 23 | 59 | 10 | 7 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0001c0005 | 0/0 | 1740 | 8 | 8 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0001c0006 | 0/0 | 1740 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0001c0009 | 0/0 | 1740 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0001c0015 | 0/0 | 1740 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0001c0017 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0002c0003 | 0/0 | 1740 | 16 | 14 | 2 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0003c0004 | 0/0 | 1740 | 12 | 5 | 2 | 5 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0003c0013 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0004c0008 | 0/0 | 1740 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0005c0007 | 0/0 | 1740 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0006c0010 | 0/0 | 1740 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0007c0011 | 0/0 | 1740 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0008c0016 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0009c0014 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 | ||
| a0010c0012 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | ATGAA others(1735): Show |
chr12 | 7299072 | 7333719 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2349 | 210 | 51 | 40 | 82 | 8 | 28 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0001t0002 | 0/0 | 2349 | 39 | 2 | 3 | 27 | 0 | 7 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0001t0003 | 0/0 | 2349 | 14 | 0 | 4 | 9 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0001t0006 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0002t0001 | 0/1 | 2349 | 110 | 11 | 23 | 58 | 10 | 7 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0002t0002 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0005t0001 | 0/0 | 2349 | 8 | 8 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0006t0005 | 0/0 | 2349 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0009t0001 | 0/0 | 2349 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0015t0001 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0001c0017t0001 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0002c0003t0004 | 0/0 | 2349 | 16 | 14 | 2 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0003c0004t0001 | 0/0 | 2349 | 12 | 5 | 2 | 5 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0003c0013t0001 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0004c0008t0003 | 0/0 | 2349 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0005c0007t0001 | 0/0 | 2349 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0006c0010t0001 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0007c0011t0002 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0008c0016t0001 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0009c0014t0001 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| a0010c0012t0001 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | TTTTT others(2344): Show |
chr12 | 7299072 | 7333719 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 41 | 2 | 16 | 10 | 4 | 9 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0003 | 0/0 | 29 | 3 | 5 | 14 | 3 | 4 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0006 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0007 | 0/0 | 12 | 10 | 1 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0009 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0014 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0018 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0030 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0010 | 0/0 | 11 | 1 | 1 | 9 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0019 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0034 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0033 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0001 | 0/0 | 45 | 0 | 1 | 43 | 1 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0004 | 0/0 | 16 | 6 | 2 | 2 | 0 | 6 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0011 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0016 | 0/1 | 6 | 0 | 3 | 0 | 2 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0036 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0005t0001g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0006t0005g0035 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0009t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0015t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0001c0017t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0002c0003t0004g0008 | 0/0 | 12 | 10 | 2 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0002c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0002c0003t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0002c0003t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0002c0003t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0003c0004t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0003c0004t0001g0017 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0003c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0003c0004t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0003c0013t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0004c0008t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0005c0007t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0005c0007t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0006c0010t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0007c0011t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0008c0016t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0009c0014t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| a0010c0012t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0140 | EUR | GBR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0037 | EUR | GBR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0047 | EUR | GBR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | FIN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0047 | EUR | FIN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0037 | EUR | FIN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01168 | hp1 | a0003 | c0004 | t0001 | g0052 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0017 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01358 | hp1 | a0002 | c0003 | t0004 | g0008 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01891 | hp1 | a0002 | c0003 | t0004 | g0008 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01952 | hp1 | a0002 | c0003 | t0004 | g0008 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0129 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CDX | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02258 | hp1 | a0002 | c0003 | t0004 | g0090 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0017 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02698 | hp2 | a0006 | c0010 | t0001 | g0025 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02717 | hp1 | a0002 | c0003 | t0004 | g0008 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02809 | hp2 | a0001 | c0006 | t0005 | g0035 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0050 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02895 | hp2 | a0002 | c0003 | t0004 | g0091 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02896 | hp1 | a0002 | c0003 | t0004 | g0008 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02897 | hp1 | a0002 | c0003 | t0004 | g0008 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02965 | hp1 | a0002 | c0003 | t0004 | g0008 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03041 | hp2 | a0002 | c0003 | t0004 | g0008 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03195 | hp1 | a0003 | c0004 | t0001 | g0017 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03209 | hp2 | a0002 | c0003 | t0004 | g0008 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03453 | hp1 | a0003 | c0004 | t0001 | g0017 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03453 | hp2 | a0002 | c0003 | t0004 | g0071 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0017 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03516 | hp2 | a0002 | c0003 | t0004 | g0008 | AFR | ESN | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03579 | hp1 | a0001 | c0017 | t0001 | g0097 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03710 | hp1 | a0007 | c0011 | t0002 | g0107 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04199 | hp1 | a0001 | c0015 | t0001 | g0037 | SAS | STU | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | YRI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | CHB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18939 | hp2 | a0008 | c0016 | t0001 | g0059 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18945 | hp2 | a0004 | c0008 | t0003 | g0015 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18963 | hp2 | a0009 | c0014 | t0001 | g0051 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18973 | hp2 | a0010 | c0012 | t0001 | g0072 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18974 | hp1 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18975 | hp1 | a0004 | c0008 | t0003 | g0015 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18981 | hp1 | a0005 | c0007 | t0001 | g0041 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18983 | hp2 | a0004 | c0008 | t0003 | g0015 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18986 | hp1 | a0001 | c0009 | t0001 | g0011 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18987 | hp1 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19005 | hp2 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19043 | hp2 | a0001 | c0006 | t0005 | g0035 | AFR | LWK | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19060 | hp1 | a0005 | c0007 | t0001 | g0041 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19064 | hp1 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19065 | hp2 | a0001 | c0009 | t0001 | g0011 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19067 | hp2 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19088 | hp2 | a0005 | c0007 | t0001 | g0005 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19240 | hp1 | a0002 | c0003 | t0004 | g0092 | AFR | YRI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | YRI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20129 | hp2 | a0001 | c0006 | t0005 | g0035 | AFR | ASW | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | TSI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0036 | EUR | TSI | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | GIH | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0008 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG06807 | hp1 | a0003 | c0013 | t0001 | g0013 | AFR | USA | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | USA | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | USA | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA21309 | hp1 | a0002 | c0003 | t0004 | g0008 | AFR | LWK | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0016 | REF | REF | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0084 | REF | REF | ACSM4_chr12_7299072_7333719 | ACSM4 | chr12 | 7299072 | 7333719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7304386 | C | T | 1 | a0004 | 3 | NA18945.hp2 NA18975.hp1 NA18983.hp2 |
missense_variant | MODERATE | c.55C>T | p.Pro19Ser | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/13 | 315/2349 | 55/1743 | 19/580 | chr12 | 7304386 | |||
| chr12:7304476 | C | T | 1 | a0005 | 3 | NA18981.hp1 NA19060.hp1 NA19088.hp2 |
missense_variant | MODERATE | c.145C>T | p.Pro49Ser | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/13 | 405/2349 | 145/1743 | 49/580 | chr12 | 7304476 | |||
| chr12:7304509 | G | A | 1 | a0006 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.178G>A | p.Asp60Asn | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/13 | 438/2349 | 178/1743 | 60/580 | chr12 | 7304509 | |||
| chr12:7306539 | G | A | 1 | a0007 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.208G>A | p.Glu70Lys | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/13 | 468/2349 | 208/1743 | 70/580 | chr12 | 7306539 | |||
| chr12:7317141 | G | A | 1 | a0010 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.625G>A | p.Ala209Thr | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/13 | 885/2349 | 625/1743 | 209/580 | chr12 | 7317141 | |||
| chr12:7322485 | C | T | 1 | a0003 | 13 | HG01168.hp1 HG01243.hp1 HG02572.hp1 others(10): Show |
stop_gained | HIGH | c.1069C>T | p.Gln357* | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/13 | 1329/2349 | 1069/1743 | 357/580 | chr12 | 7322485 | |||
| chr12:7322534 | C | T | 1 | a0008 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.1118C>T | p.Thr373Met | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/13 | 1378/2349 | 1118/1743 | 373/580 | chr12 | 7322534 | |||
| chr12:7323549 | T | G | 1 | a0010 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.1297T>G | p.Ser433Ala | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 9/13 | 1557/2349 | 1297/1743 | 433/580 | chr12 | 7323549 | |||
| chr12:7324504 | G | A | 1 | a0002 | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
missense_variant | MODERATE | c.1442G>A | p.Arg481His | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/13 | 1702/2349 | 1442/1743 | 481/580 | chr12 | 7324504 | |||
| chr12:7327004 | C | A | 1 | a0009 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.1565C>A | p.Ala522Glu | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/13 | 1825/2349 | 1565/1743 | 522/580 | chr12 | 7327004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7306685 | C | T | 1 | a0001c0017 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.354C>T | p.Ala118Ala | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/13 | 614/2349 | 354/1743 | 118/580 | chr12 | 7306685 | |||
| chr12:7306698 | A | C | 2 | a0001c0005a0001c0006 | 11 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
synonymous_variant | LOW | c.367A>C | p.Arg123Arg | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/13 | 627/2349 | 367/1743 | 123/580 | chr12 | 7306698 | |||
| chr12:7310543 | C | T | 1 | a0001c0009 | 2 | NA18986.hp1 NA19065.hp2 |
synonymous_variant | LOW | c.417C>T | p.Ile139Ile | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/13 | 677/2349 | 417/1743 | 139/580 | chr12 | 7310543 | |||
| chr12:7310645 | A | T | 5 | a0001c0002a0001c0009a0001c0015others(2): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
synonymous_variant | LOW | c.519A>T | p.Pro173Pro | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/13 | 779/2349 | 519/1743 | 173/580 | chr12 | 7310645 | |||
| chr12:7318092 | C | T | 1 | a0001c0006 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.831C>T | p.Ala277Ala | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/13 | 1091/2349 | 831/1743 | 277/580 | chr12 | 7318092 | |||
| chr12:7318131 | C | T | 1 | a0008c0016 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.870C>T | p.Ala290Ala | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/13 | 1130/2349 | 870/1743 | 290/580 | chr12 | 7318131 | |||
| chr12:7322451 | C | T | 1 | a0001c0015 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1035C>T | p.Thr345Thr | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/13 | 1295/2349 | 1035/1743 | 345/580 | chr12 | 7322451 | |||
| chr12:7323531 | C | A | 1 | a0003c0013 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1279C>A | p.Arg427Arg | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 9/13 | 1539/2349 | 1279/1743 | 427/580 | chr12 | 7323531 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7304167 | T | C | 1 | a0001c0001t0006 | 1 | HG00544.hp2 | 5_prime_UTR_variant | MODIFIER | c.-165T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/13 | 165 | chr12 | 7304167 | ||||||
| chr12:7328489 | T | C | 5 | a0001c0001t0002a0001c0001t0003a0001c0002t0002others(2): Show | 58 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*116T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 13/13 | 116 | chr12 | 7328489 | ||||||
| chr12:7328554 | C | T | 7 | a0001c0001t0002a0001c0001t0003a0001c0002t0002others(4): Show | 77 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*181C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 13/13 | 181 | chr12 | 7328554 | ||||||
| chr12:7328595 | T | C | 1 | a0002c0003t0004 | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*222T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 13/13 | 222 | chr12 | 7328595 | ||||||
| chr12:7328649 | A | G | 2 | a0001c0001t0003a0004c0008t0003 | 17 | HG00597.hp1 HG01928.hp1 HG01975.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*276A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 13/13 | 276 | chr12 | 7328649 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7304596 | T | C | 18 | a0001c0001t0001g0049a0001c0002t0001g0001a0001c0002t0001g0023others(15): Show | 74 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.201+64T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7304596 | |||||||
| chr12:7304597 | T | A | 1 | a0001c0002t0001g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.201+65T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7304597 | |||||||
| chr12:7304621 | C | T | 22 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0016others(19): Show | 54 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.201+89C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7304621 | |||||||
| chr12:7304666 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.201+134A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7304666 | |||||||
| chr12:7304690 | A | C | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.201+158A>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7304690 | |||||||
| chr12:7304759 | C | T | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.201+227C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7304759 | |||||||
| chr12:7304760 | G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0130 | 2 | HG03516.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.201+228G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7304760 | |||||||
| chr12:7304891 | T | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0020others(14): Show | 68 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.201+359T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7304891 | |||||||
| chr12:7305064 | C | T | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.201+532C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305064 | |||||||
| chr12:7305082 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.201+550T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305082 | |||||||
| chr12:7305153 | C | A | 1 | a0005c0007t0001g0041 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.201+621C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305153 | |||||||
| chr12:7305222 | G | A | 1 | a0001c0002t0001g0045 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.201+690G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305222 | |||||||
| chr12:7305463 | G | T | 40 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0108others(37): Show | 89 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.201+931G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305463 | |||||||
| chr12:7305701 | C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0070others(12): Show | 55 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.202-832C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305701 | |||||||
| chr12:7305725 | G | A | 1 | a0002c0003t0004g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.202-808G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305725 | |||||||
| chr12:7305738 | G | C | 3 | a0001c0001t0001g0049a0003c0004t0001g0017a0003c0004t0001g0050 | 7 | HG01243.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-795G>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305738 | |||||||
| chr12:7305764 | G | A | 3 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0105 | 7 | HG02056.hp1 HG02132.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-769G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305764 | |||||||
| chr12:7305831 | A | C | 1 | a0001c0001t0001g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.202-702A>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7305831 | |||||||
| chr12:7306147 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.202-386A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7306147 | |||||||
| chr12:7306328 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.202-205C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 1/12 | chr12 | 7306328 | |||||||
| chr12:7306842 | G | A | 1 | a0010c0012t0001g0072 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.412+99G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7306842 | |||||||
| chr12:7306847 | C | CA | 28 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(25): Show | 91 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.412+121dupA | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 7306847 | ||||||
| chr12:7306847 | C | CAA | 18 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0020others(15): Show | 66 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.412+120_412+121dup others(2): Show |
ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 7306847 | ||||||
| chr12:7306847 | CA | C | 44 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(41): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.412+121delA | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 7306847 | ||||||
| chr12:7306847 | CAA | C | 7 | a0001c0001t0001g0089a0001c0006t0005g0035a0002c0003t0004g0008others(4): Show | 20 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.412+120_412+121del others(2): Show |
ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 7306847 | ||||||
| chr12:7306977 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.412+234G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7306977 | |||||||
| chr12:7307171 | G | A | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412+428G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7307171 | |||||||
| chr12:7307593 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.412+850A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7307593 | |||||||
| chr12:7307737 | T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0027others(3): Show | 17 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.412+994T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7307737 | |||||||
| chr12:7307880 | A | G | 2 | a0001c0005t0001g0012a0001c0005t0001g0129 | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.412+1137A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7307880 | |||||||
| chr12:7307964 | T | C | 1 | a0001c0002t0001g0038 | 2 | NA18990.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.412+1221T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7307964 | |||||||
| chr12:7307995 | G | A | 1 | a0007c0011t0002g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.412+1252G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7307995 | |||||||
| chr12:7308040 | GC | G | 1 | a0001c0001t0001g0020 | 4 | HG01943.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+1298delC | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308040 | |||||||
| chr12:7308137 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.412+1394G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308137 | |||||||
| chr12:7308187 | C | T | 1 | a0010c0012t0001g0072 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.412+1444C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308187 | |||||||
| chr12:7308227 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412+1484T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308227 | |||||||
| chr12:7308272 | T | C | 1 | a0003c0004t0001g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.412+1529T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308272 | |||||||
| chr12:7308310 | T | C | 2 | a0001c0005t0001g0012a0001c0005t0001g0129 | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.412+1567T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308310 | |||||||
| chr12:7308411 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.412+1668C>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308411 | |||||||
| chr12:7308490 | T | C | 2 | a0001c0002t0001g0045a0001c0002t0001g0131 | 3 | HG02976.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412+1747T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308490 | |||||||
| chr12:7308522 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.412+1779C>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308522 | |||||||
| chr12:7308645 | G | A | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413-1894G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308645 | |||||||
| chr12:7308674 | T | C | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413-1865T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7308674 | |||||||
| chr12:7309008 | G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(16): Show | 60 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.413-1531G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309008 | |||||||
| chr12:7309199 | G | A | 35 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(32): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.413-1340G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309199 | |||||||
| chr12:7309762 | C | G | 1 | a0001c0002t0001g0140 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.413-777C>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309762 | |||||||
| chr12:7309887 | G | T | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413-652G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309887 | |||||||
| chr12:7309905 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.413-634T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309905 | |||||||
| chr12:7309924 | T | G | 1 | a0001c0002t0001g0023 | 3 | HG00621.hp1 NA18978.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.413-615T>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309924 | |||||||
| chr12:7309932 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.413-607C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309932 | |||||||
| chr12:7309933 | G | A | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413-606G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309933 | |||||||
| chr12:7309972 | C | A | 1 | a0001c0001t0002g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.413-567C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309972 | |||||||
| chr12:7309980 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413-559C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7309980 | |||||||
| chr12:7310036 | C | T | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413-503C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7310036 | |||||||
| chr12:7310088 | G | A | 36 | a0001c0001t0001g0083a0001c0002t0001g0001a0001c0002t0001g0004others(33): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.413-451G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7310088 | |||||||
| chr12:7310190 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.413-349A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7310190 | |||||||
| chr12:7310368 | A | G | 2 | a0001c0005t0001g0012a0001c0005t0001g0129 | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.413-171A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7310368 | |||||||
| chr12:7310395 | T | C | 1 | a0001c0002t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.413-144T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7310395 | |||||||
| chr12:7310526 | C | T | 6 | a0001c0001t0001g0130a0002c0003t0004g0008a0002c0003t0004g0071others(3): Show | 17 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.413-13C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 2/12 | chr12 | 7310526 | |||||||
| chr12:7310802 | T | C | 34 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0116others(31): Show | 70 | HG00597.hp1 HG00639.hp1 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.620+56T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7310802 | |||||||
| chr12:7310895 | C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(142): Show | 425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
intron_variant | MODIFIER | c.620+149C>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7310895 | |||||||
| chr12:7310982 | G | A | 2 | a0001c0005t0001g0012a0001c0005t0001g0129 | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.620+236G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7310982 | |||||||
| chr12:7311173 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.620+427T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311173 | |||||||
| chr12:7311194 | T | G | 9 | a0001c0001t0001g0130a0001c0001t0002g0019a0001c0005t0001g0012others(6): Show | 30 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(27): Show |
intron_variant | MODIFIER | c.620+448T>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311194 | |||||||
| chr12:7311208 | A | G | 1 | a0001c0001t0002g0032 | 3 | HG02056.hp1 HG02523.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.620+462A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311208 | |||||||
| chr12:7311210 | G | T | 34 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0116others(31): Show | 70 | HG00597.hp1 HG00639.hp1 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.620+464G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311210 | |||||||
| chr12:7311275 | C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(22): Show | 89 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.620+529C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311275 | |||||||
| chr12:7311537 | G | A | 2 | a0001c0005t0001g0012a0001c0005t0001g0129 | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.620+791G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311537 | |||||||
| chr12:7311563 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.620+817G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311563 | |||||||
| chr12:7311683 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.620+937G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311683 | |||||||
| chr12:7311698 | G | T | 7 | a0001c0001t0003g0015a0001c0001t0003g0044a0001c0001t0003g0123others(4): Show | 13 | HG00597.hp1 HG03130.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.620+952G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311698 | |||||||
| chr12:7311739 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.620+993A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311739 | |||||||
| chr12:7311933 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.620+1187C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7311933 | |||||||
| chr12:7312017 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.620+1271G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7312017 | |||||||
| chr12:7312140 | A | C | 32 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0116others(29): Show | 62 | HG00597.hp1 HG00639.hp1 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.620+1394A>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7312140 | |||||||
| chr12:7312287 | C | T | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.620+1541C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7312287 | |||||||
| chr12:7312291 | A | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(60): Show | 159 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.620+1545A>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7312291 | |||||||
| chr12:7312506 | A | G | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.620+1760A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7312506 | |||||||
| chr12:7312550 | A | G | 27 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(24): Show | 91 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.620+1804A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7312550 | |||||||
| chr12:7312653 | T | C | 1 | a0001c0002t0001g0054 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.620+1907T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7312653 | |||||||
| chr12:7312981 | A | T | 1 | a0001c0002t0001g0139 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.620+2235A>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7312981 | |||||||
| chr12:7313082 | T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0088 | 2 | HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.620+2336T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7313082 | |||||||
| chr12:7313135 | C | A | 1 | a0001c0001t0001g0042 | 2 | NA18967.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.620+2389C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7313135 | |||||||
| chr12:7313239 | G | A | 6 | a0001c0006t0005g0035a0002c0003t0004g0008a0002c0003t0004g0071others(3): Show | 19 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.620+2493G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7313239 | |||||||
| chr12:7313345 | G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0020others(14): Show | 68 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.620+2599G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7313345 | |||||||
| chr12:7313416 | A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0088a0010c0012t0001g0072 | 3 | HG03239.hp2 NA18973.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.620+2670A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7313416 | |||||||
| chr12:7313573 | T | C | 1 | a0002c0003t0004g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.620+2827T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7313573 | |||||||
| chr12:7314370 | T | C | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.621-2767T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7314370 | |||||||
| chr12:7314512 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.621-2625T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7314512 | |||||||
| chr12:7314602 | T | C | 1 | a0001c0001t0001g0024 | 3 | HG00738.hp1 HG01074.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.621-2535T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7314602 | |||||||
| chr12:7314606 | T | TGATA | 28 | a0001c0001t0001g0108a0001c0001t0001g0116a0001c0001t0002g0010others(25): Show | 56 | HG00597.hp1 HG00639.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.621-2512_621-2509d others(6): Show |
ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 7314606 | ||||||
| chr12:7314692 | G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0093a0001c0001t0001g0096 | 3 | HG01099.hp2 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.621-2445G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7314692 | |||||||
| chr12:7314713 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.621-2424G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7314713 | |||||||
| chr12:7314777 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.621-2360T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7314777 | |||||||
| chr12:7314813 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.621-2324G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7314813 | |||||||
| chr12:7314948 | T | C | 31 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0116others(28): Show | 59 | HG00597.hp1 HG00639.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.621-2189T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7314948 | |||||||
| chr12:7315037 | A | C | 1 | a0001c0002t0001g0139 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.621-2100A>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315037 | |||||||
| chr12:7315163 | T | C | 1 | a0001c0001t0003g0044 | 2 | HG00597.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.621-1974T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315163 | |||||||
| chr12:7315195 | C | CA | 9 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0110others(6): Show | 9 | HG00741.hp2 HG01071.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.621-1925dupA | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 7315195 | ||||||
| chr12:7315195 | CA | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0067others(2): Show | 10 | HG01168.hp2 HG01243.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.621-1925delA | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 7315195 | ||||||
| chr12:7315348 | C | T | 6 | a0001c0001t0001g0049a0003c0004t0001g0013a0003c0004t0001g0017others(3): Show | 14 | HG01168.hp1 HG01243.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.621-1789C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315348 | |||||||
| chr12:7315349 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.621-1788G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315349 | |||||||
| chr12:7315494 | C | T | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.621-1643C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315494 | |||||||
| chr12:7315622 | A | T | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.621-1515A>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315622 | |||||||
| chr12:7315680 | C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0088 | 2 | HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.621-1457C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315680 | |||||||
| chr12:7315754 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.621-1383A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315754 | |||||||
| chr12:7315873 | G | T | 2 | a0001c0005t0001g0012a0001c0005t0001g0129 | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-1264G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315873 | |||||||
| chr12:7315874 | C | G | 2 | a0001c0005t0001g0012a0001c0005t0001g0129 | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-1263C>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315874 | |||||||
| chr12:7315937 | A | G | 1 | a0001c0001t0002g0121 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.621-1200A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7315937 | |||||||
| chr12:7316022 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.621-1115A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7316022 | |||||||
| chr12:7316392 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.621-745G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7316392 | |||||||
| chr12:7316517 | G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(19): Show | 84 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.621-620G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7316517 | |||||||
| chr12:7316651 | C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(111): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.621-486C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7316651 | |||||||
| chr12:7316865 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.621-272T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7316865 | |||||||
| chr12:7316964 | C | T | 2 | a0001c0005t0001g0012a0001c0005t0001g0129 | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-173C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7316964 | |||||||
| chr12:7317047 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.621-90C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7317047 | |||||||
| chr12:7317107 | C | A | 3 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0135 | 3 | NA18998.hp2 NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.621-30C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 3/12 | chr12 | 7317107 | |||||||
| chr12:7317286 | G | A | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.764+6G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/12 | chr12 | 7317286 | |||||||
| chr12:7317423 | G | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0070others(12): Show | 55 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.764+143G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/12 | chr12 | 7317423 | |||||||
| chr12:7317468 | G | A | 1 | a0001c0002t0001g0036 | 3 | HG01175.hp2 HG01255.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.764+188G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/12 | chr12 | 7317468 | |||||||
| chr12:7317615 | G | C | 1 | a0001c0001t0002g0117 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.764+335G>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/12 | chr12 | 7317615 | |||||||
| chr12:7317746 | C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0070others(15): Show | 58 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.765-280C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/12 | chr12 | 7317746 | |||||||
| chr12:7317937 | T | C | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.765-89T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/12 | chr12 | 7317937 | |||||||
| chr12:7317938 | A | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(113): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.765-88A>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/12 | chr12 | 7317938 | |||||||
| chr12:7317970 | T | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(21): Show | 86 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.765-56T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 4/12 | chr12 | 7317970 | |||||||
| chr12:7318256 | T | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0086 | 16 | HG00609.hp2 HG00621.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.921+74T>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318256 | |||||||
| chr12:7318345 | G | C | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.921+163G>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318345 | |||||||
| chr12:7318373 | A | T | 1 | a0001c0002t0001g0138 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.921+191A>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318373 | |||||||
| chr12:7318505 | T | A | 1 | a0001c0001t0003g0125 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.921+323T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318505 | |||||||
| chr12:7318511 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.921+329T>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318511 | |||||||
| chr12:7318558 | A | C | 3 | a0003c0004t0001g0013a0003c0004t0001g0052a0003c0013t0001g0013 | 7 | HG01168.hp1 HG06807.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+376A>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318558 | |||||||
| chr12:7318651 | C | T | 5 | a0001c0001t0001g0078a0001c0002t0001g0011a0001c0002t0001g0047others(2): Show | 12 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.921+469C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318651 | |||||||
| chr12:7318785 | C | A | 6 | a0001c0001t0003g0015a0001c0001t0003g0044a0001c0001t0003g0123others(3): Show | 11 | HG00597.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.921+603C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318785 | |||||||
| chr12:7318936 | C | T | 29 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0031others(26): Show | 57 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.921+754C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318936 | |||||||
| chr12:7318954 | C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0078 | 4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.921+772C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7318954 | |||||||
| chr12:7319032 | T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0073others(1): Show | 13 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.921+850T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319032 | |||||||
| chr12:7319053 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.921+871C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319053 | |||||||
| chr12:7319497 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.922-1228A>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319497 | |||||||
| chr12:7319610 | A | G | 1 | a0001c0002t0001g0137 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.922-1115A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319610 | |||||||
| chr12:7319628 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.922-1097C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319628 | |||||||
| chr12:7319661 | T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0078 | 4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.922-1064T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319661 | |||||||
| chr12:7319713 | TG | T | 1 | a0001c0005t0001g0012 | 7 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.922-1008delG | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 7319713 | ||||||
| chr12:7319747 | A | G | 2 | a0001c0001t0002g0120a0007c0011t0002g0107 | 2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.922-978A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319747 | |||||||
| chr12:7319967 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.922-758C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319967 | |||||||
| chr12:7319977 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.922-748A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7319977 | |||||||
| chr12:7320036 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.922-689G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7320036 | |||||||
| chr12:7320113 | A | G | 24 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(21): Show | 86 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.922-612A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7320113 | |||||||
| chr12:7320224 | A | AT | 29 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0031others(26): Show | 57 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.922-496dupT | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 7320224 | ||||||
| chr12:7320351 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.922-374A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7320351 | |||||||
| chr12:7320502 | T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0116 | 3 | HG02109.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.922-223T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7320502 | |||||||
| chr12:7320542 | T | C | 1 | a0001c0017t0001g0097 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.922-183T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7320542 | |||||||
| chr12:7320617 | C | T | 2 | a0001c0001t0001g0126a0008c0016t0001g0059 | 2 | HG02074.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.922-108C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7320617 | |||||||
| chr12:7320642 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.922-83A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 5/12 | chr12 | 7320642 | |||||||
| chr12:7320815 | A | G | 1 | a0001c0001t0001g0028 | 3 | HG01884.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1001+11A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7320815 | |||||||
| chr12:7321072 | G | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0078 | 4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+268G>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7321072 | |||||||
| chr12:7321233 | C | T | 2 | a0001c0002t0001g0057a0001c0002t0001g0135 | 2 | NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1001+429C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7321233 | |||||||
| chr12:7321480 | G | A | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1001+676G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7321480 | |||||||
| chr12:7321518 | A | T | 31 | a0001c0001t0001g0089a0001c0001t0002g0010a0001c0001t0002g0019others(28): Show | 59 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1001+714A>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7321518 | |||||||
| chr12:7321573 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1001+769G>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7321573 | |||||||
| chr12:7321900 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1002-518T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7321900 | |||||||
| chr12:7322036 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1002-382A>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7322036 | |||||||
| chr12:7322253 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1002-165C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7322253 | |||||||
| chr12:7322406 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1002-12C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 6/12 | chr12 | 7322406 | |||||||
| chr12:7322576 | G | T | 1 | a0001c0002t0001g0137 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1125+35G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7322576 | |||||||
| chr12:7322578 | G | T | 1 | a0001c0002t0001g0137 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1125+37G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7322578 | |||||||
| chr12:7322603 | A | G | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1125+62A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7322603 | |||||||
| chr12:7322699 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1125+158T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7322699 | |||||||
| chr12:7322779 | G | A | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1125+238G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7322779 | |||||||
| chr12:7322819 | T | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0088 | 2 | HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1125+278T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7322819 | |||||||
| chr12:7322850 | C | T | 30 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0031others(27): Show | 58 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1125+309C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7322850 | |||||||
| chr12:7323014 | T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0070others(15): Show | 58 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1126-220T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7323014 | |||||||
| chr12:7323039 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1126-195C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7323039 | |||||||
| chr12:7323086 | A | G | 1 | a0002c0003t0004g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1126-148A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7323086 | |||||||
| chr12:7323123 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1126-111C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 7/12 | chr12 | 7323123 | |||||||
| chr12:7323349 | G | A | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1206+35G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 8/12 | chr12 | 7323349 | |||||||
| chr12:7323395 | A | G | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1207-64A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 8/12 | chr12 | 7323395 | |||||||
| chr12:7323412 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1207-47T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 8/12 | chr12 | 7323412 | |||||||
| chr12:7323641 | C | T | 3 | a0001c0001t0002g0034a0001c0001t0002g0112a0001c0001t0002g0128 | 5 | HG01074.hp2 HG01496.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+81C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 9/12 | chr12 | 7323641 | |||||||
| chr12:7324026 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1309-247C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 9/12 | chr12 | 7324026 | |||||||
| chr12:7324126 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1309-147A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 9/12 | chr12 | 7324126 | |||||||
| chr12:7324139 | G | C | 1 | a0001c0001t0002g0128 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1309-134G>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 9/12 | chr12 | 7324139 | |||||||
| chr12:7324155 | C | CA | 11 | a0001c0001t0001g0049a0001c0001t0001g0069a0001c0001t0002g0043others(8): Show | 21 | HG00140.hp1 HG00323.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1309-105dupA | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 7324155 | ||||||
| chr12:7324675 | C | A | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1536+77C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7324675 | |||||||
| chr12:7324702 | G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0070others(93): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1536+104G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7324702 | |||||||
| chr12:7324832 | TA | T | 38 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0063others(35): Show | 81 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1536+249delA | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 7324832 | ||||||
| chr12:7324874 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1536+276A>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7324874 | |||||||
| chr12:7324967 | G | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(142): Show | 425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
intron_variant | MODIFIER | c.1536+369G>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7324967 | |||||||
| chr12:7324994 | C | A | 1 | a0001c0002t0001g0055 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1536+396C>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7324994 | |||||||
| chr12:7325035 | C | G | 6 | a0001c0001t0001g0049a0003c0004t0001g0013a0003c0004t0001g0017others(3): Show | 14 | HG01168.hp1 HG01243.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1536+437C>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325035 | |||||||
| chr12:7325152 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1536+554G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325152 | |||||||
| chr12:7325202 | T | A | 1 | a0001c0002t0001g0039 | 2 | HG00544.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1536+604T>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325202 | |||||||
| chr12:7325269 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1536+671C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325269 | |||||||
| chr12:7325296 | C | T | 30 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0031others(27): Show | 58 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1536+698C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325296 | |||||||
| chr12:7325354 | A | G | 2 | a0001c0001t0003g0033a0001c0001t0003g0106 | 4 | HG01928.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536+756A>G | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325354 | |||||||
| chr12:7325445 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1536+847G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325445 | |||||||
| chr12:7325842 | T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0070others(15): Show | 58 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1537-1134T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325842 | |||||||
| chr12:7325872 | C | T | 1 | a0007c0011t0002g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1537-1104C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325872 | |||||||
| chr12:7325881 | C | T | 2 | a0001c0001t0001g0025a0006c0010t0001g0025 | 3 | HG02698.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1537-1095C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325881 | |||||||
| chr12:7325907 | G | A | 35 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0031others(32): Show | 74 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1537-1069G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7325907 | |||||||
| chr12:7326023 | A | C | 5 | a0002c0003t0004g0008a0002c0003t0004g0071a0002c0003t0004g0090others(2): Show | 16 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1537-953A>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7326023 | |||||||
| chr12:7326108 | G | A | 5 | a0001c0002t0001g0016a0001c0002t0001g0037a0001c0002t0001g0058others(2): Show | 10 | HG00140.hp1 HG00323.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1537-868G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7326108 | |||||||
| chr12:7326398 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1537-578T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7326398 | |||||||
| chr12:7326513 | T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(15): Show | 59 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1537-463T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 11/12 | chr12 | 7326513 | |||||||
| chr12:7327183 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1656+88G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | chr12 | 7327183 | |||||||
| chr12:7327300 | C | T | 1 | a0001c0001t0001g0029 | 3 | HG03017.hp2 HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1656+205C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | chr12 | 7327300 | |||||||
| chr12:7327532 | T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(20): Show | 85 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.1656+437T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | chr12 | 7327532 | |||||||
| chr12:7327582 | C | T | 30 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0031others(27): Show | 58 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1656+487C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | chr12 | 7327582 | |||||||
| chr12:7327729 | TTCACTAA others(14): Show |
T | 1 | a0001c0002t0001g0047 | 2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.1657-546_1657-526d others(23): Show |
ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 7327729 | ||||||
| chr12:7327883 | T | C | 1 | a0001c0006t0005g0035 | 3 | HG02809.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1657-404T>C | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | chr12 | 7327883 | |||||||
| chr12:7327887 | C | T | 3 | a0003c0004t0001g0013a0003c0004t0001g0052a0003c0013t0001g0013 | 7 | HG01168.hp1 HG06807.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1657-400C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | chr12 | 7327887 | |||||||
| chr12:7327987 | G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0074 | 7 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1657-300G>A | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | chr12 | 7327987 | |||||||
| chr12:7328122 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1657-165C>T | ACSM4 | ENSG00000215009.6 | transcript | ENST00000399422.5 | protein_coding | 12/12 | chr12 | 7328122 |