Search by Gene
| Item | Value |
|---|---|
| geneid | 6296 |
| ensemblid | ENSG00000005187.12 |
| hgncid | 10522 |
| symbol | ACSM3 |
| name | acyl-CoA synthetase medium chain family member 3 |
| refseq_nuc | NM_005622.4 |
| refseq_prot | NP_005613.2 |
| ensembl_nuc | ENST00000289416.10 |
| ensembl_prot | ENSP00000289416.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 20764014 |
| end | 20797581 |
| strand | + |
| ver | v1.2 |
| region | chr16:20764014-20797581 |
| region5000 | chr16:20759014-20802581 |
| regionname0 | ACSM3_chr16_20764014_20797581 |
| regionname5000 | ACSM3_chr16_20759014_20802581 |
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 | 586 | 286 | 72 | 52 | 112 | 12 | 36 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0002 | 0/0 | 586 | 40 | 1 | 3 | 32 | 0 | 4 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0003 | 0/0 | 586 | 13 | 13 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0004 | 0/0 | 330 | 6 | 4 | 2 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(325): Show |
chr16 | 20759014 | 20802581 |
| a0005 | 0/0 | 586 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0006 | 0/0 | 586 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0007 | 0/0 | 586 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0008 | 0/0 | 586 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0009 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0010 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| a0011 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | MLARV others(581): Show |
chr16 | 20759014 | 20802581 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1758 | 271 | 58 | 51 | 112 | 12 | 36 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0001c0004 | 0/0 | 1758 | 10 | 10 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0001c0008 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0001c0012 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0001c0016 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0001c0017 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0002c0002 | 0/0 | 1758 | 40 | 1 | 3 | 32 | 0 | 4 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0003c0003 | 0/0 | 1758 | 13 | 13 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0004c0005 | 0/0 | 1758 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0004c0013 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0004c0015 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0005c0006 | 0/0 | 1758 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0006c0009 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0007c0007 | 0/0 | 1758 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0008c0018 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0009c0014 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0010c0011 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 | ||
| a0011c0010 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | ATGCT others(1753): Show |
chr16 | 20759014 | 20802581 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2533 | 262 | 51 | 51 | 111 | 12 | 35 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0001c0001t0002 | 0/0 | 2533 | 7 | 7 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0001c0001t0004 | 0/0 | 2533 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0001c0001t0005 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0001c0004t0001 | 0/0 | 2533 | 10 | 10 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0001c0008t0001 | 0/0 | 2533 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0001c0012t0001 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0001c0016t0001 | 0/0 | 2533 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0001c0017t0001 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0002c0002t0001 | 0/0 | 2533 | 39 | 1 | 3 | 31 | 0 | 4 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0002c0002t0003 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0003c0003t0001 | 0/0 | 2533 | 13 | 13 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0004c0005t0001 | 0/0 | 2533 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0004c0013t0001 | 0/0 | 2533 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0004c0015t0001 | 0/0 | 2533 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0005c0006t0001 | 0/0 | 2533 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0006c0009t0001 | 0/0 | 2533 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0007c0007t0001 | 0/0 | 2533 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0008c0018t0001 | 0/0 | 2533 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0009c0014t0001 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0010c0011t0001 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| a0011c0010t0001 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | CTTCT others(2528): Show |
chr16 | 20759014 | 20802581 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 0 | 3 | 20 | 1 | 4 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0002 | 0/0 | 24 | 1 | 6 | 12 | 1 | 4 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0004 | 1/1 | 7 | 3 | 2 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0007 | 0/0 | 7 | 1 | 5 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 2 | 1 | 1 | 3 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0004t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0008t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0012t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0016t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0001c0017t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0003 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0003c0003t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0003c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0003c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0003c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0003c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0003c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0003c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0003c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0004c0005t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0004c0005t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0004c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0004c0013t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0004c0015t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0005c0006t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0005c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0006c0009t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0007c0007t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0007c0007t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0008c0018t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0009c0014t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0010c0011t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| a0011c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00733 | hp1 | a0008 | c0018 | t0001 | g0001 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01099 | hp2 | a0001 | c0016 | t0001 | g0068 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01243 | hp2 | a0004 | c0015 | t0001 | g0002 | AMR | PUR | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01358 | hp2 | a0004 | c0013 | t0001 | g0027 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01891 | hp1 | a0001 | c0017 | t0001 | g0013 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02056 | hp1 | a0009 | c0014 | t0001 | g0003 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02074 | hp2 | a0010 | c0011 | t0001 | g0131 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | CDX | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0064 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0061 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0023 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02622 | hp1 | a0004 | c0005 | t0001 | g0048 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0063 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0062 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0060 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02965 | hp1 | a0001 | c0008 | t0001 | g0030 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02965 | hp2 | a0004 | c0005 | t0001 | g0182 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03098 | hp1 | a0001 | c0012 | t0001 | g0189 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0055 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03195 | hp1 | a0004 | c0005 | t0001 | g0048 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03225 | hp2 | a0001 | c0008 | t0001 | g0030 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03516 | hp2 | a0004 | c0005 | t0001 | g0186 | AFR | ESN | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0106 | SAS | STU | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03704 | hp2 | a0007 | c0007 | t0001 | g0095 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | BEB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03927 | hp2 | a0007 | c0007 | t0001 | g0096 | SAS | BEB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0017 | SAS | BEB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0065 | AFR | YRI | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18947 | hp2 | a0005 | c0006 | t0001 | g0003 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18987 | hp2 | a0011 | c0010 | t0001 | g0127 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18989 | hp2 | a0005 | c0006 | t0001 | g0003 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18995 | hp1 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19005 | hp1 | a0005 | c0006 | t0001 | g0116 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0059 | AFR | LWK | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | GIH | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02486 | hp2 | a0006 | c0009 | t0001 | g0051 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG03471 | hp2 | a0006 | c0009 | t0001 | g0051 | AFR | MSL | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | USA | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0004 | REF | REF | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | ACSM3_chr16_20759014_20802581 | ACSM3 | chr16 | 20759014 | 20802581 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:20770095 | A | G | 1 | a0006 | 2 | HG02486.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.61A>G | p.Ile21Val | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/14 | 224/2533 | 61/1761 | 21/586 | chr16 | 20770095 | |||
| chr16:20770102 | G | A | 1 | a0011 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.68G>A | p.Gly23Asp | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/14 | 231/2533 | 68/1761 | 23/586 | chr16 | 20770102 | |||
| chr16:20770167 | T | C | 1 | a0007 | 2 | HG03704.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.133T>C | p.Ser45Pro | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/14 | 296/2533 | 133/1761 | 45/586 | chr16 | 20770167 | |||
| chr16:20780999 | G | C | 1 | a0005 | 3 | NA18947.hp2 NA18989.hp2 NA19005.hp1 |
missense_variant | MODERATE | c.808G>C | p.Asp270His | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/14 | 971/2533 | 808/1761 | 270/586 | chr16 | 20780999 | |||
| chr16:20781066 | G | A | 1 | a0004 | 4 | HG02622.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
stop_gained | HIGH | c.875G>A | p.Trp292* | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/14 | 1038/2533 | 875/1761 | 292/586 | chr16 | 20781066 | |||
| chr16:20781095 | C | T | 1 | a0008 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.904C>T | p.His302Tyr | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/14 | 1067/2533 | 904/1761 | 302/586 | chr16 | 20781095 | |||
| chr16:20781113 | C | A | 1 | a0003 | 13 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
missense_variant | MODERATE | c.922C>A | p.Pro308Thr | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/14 | 1085/2533 | 922/1761 | 308/586 | chr16 | 20781113 | |||
| chr16:20781759 | C | T | 1 | a0004 | 1 | HG01243.hp2 | stop_gained | HIGH | c.991C>T | p.Arg331* | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/14 | 1154/2533 | 991/1761 | 331/586 | chr16 | 20781759 | |||
| chr16:20781762 | A | G | 1 | a0009 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.994A>G | p.Met332Val | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/14 | 1157/2533 | 994/1761 | 332/586 | chr16 | 20781762 | |||
| chr16:20785065 | G | C | 3 | a0002a0005a0009 | 44 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(41): Show |
missense_variant | MODERATE | c.1101G>C | p.Lys367Asn | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 8/14 | 1264/2533 | 1101/1761 | 367/586 | chr16 | 20785065 | |||
| chr16:20790685 | C | G | 1 | a0004 | 1 | HG01358.hp2 | stop_gained | HIGH | c.1323C>G | p.Tyr441* | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 10/14 | 1486/2533 | 1323/1761 | 441/586 | chr16 | 20790685 | |||
| chr16:20792069 | T | C | 1 | a0010 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.1394T>C | p.Met465Thr | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 11/14 | 1557/2533 | 1394/1761 | 465/586 | chr16 | 20792069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:20770235 | A | G | 1 | a0007c0007 | 2 | HG03704.hp2 HG03927.hp2 |
synonymous_variant | LOW | c.201A>G | p.Gln67Gln | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/14 | 364/2533 | 201/1761 | 67/586 | chr16 | 20770235 | |||
| chr16:20777530 | T | C | 2 | a0001c0004a0003c0003 | 23 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
synonymous_variant | LOW | c.588T>C | p.Ile196Ile | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/14 | 751/2533 | 588/1761 | 196/586 | chr16 | 20777530 | |||
| chr16:20781103 | C | T | 1 | a0001c0017 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.912C>T | p.Pro304Pro | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/14 | 1075/2533 | 912/1761 | 304/586 | chr16 | 20781103 | |||
| chr16:20781758 | C | T | 1 | a0001c0016 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.990C>T | p.Tyr330Tyr | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/14 | 1153/2533 | 990/1761 | 330/586 | chr16 | 20781758 | |||
| chr16:20786149 | C | T | 1 | a0001c0008 | 2 | HG02965.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.1215C>T | p.Phe405Phe | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/14 | 1378/2533 | 1215/1761 | 405/586 | chr16 | 20786149 | |||
| chr16:20792115 | C | T | 1 | a0006c0009 | 2 | HG02486.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.1440C>T | p.Val480Val | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 11/14 | 1603/2533 | 1440/1761 | 480/586 | chr16 | 20792115 | |||
| chr16:20792236 | C | T | 1 | a0001c0012 | 1 | HG03098.hp1 | splice_region_variant&synonymous_variant | LOW | c.1455C>T | p.Gly485Gly | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/14 | 1618/2533 | 1455/1761 | 485/586 | chr16 | 20792236 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:20764040 | G | A | 1 | a0002c0002t0003 | 1 | NA18995.hp1 | 5_prime_UTR_variant | MODIFIER | c.-137G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/14 | 5995 | chr16 | 20764040 | ||||||
| chr16:20770008 | T | C | 1 | a0001c0001t0002 | 7 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-27T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/14 | 27 | chr16 | 20770008 | ||||||
| chr16:20797088 | A | C | 1 | a0001c0001t0005 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 14/14 | 116 | chr16 | 20797088 | ||||||
| chr16:20797429 | T | C | 1 | a0001c0001t0004 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*457T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 14/14 | 457 | chr16 | 20797429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:20764289 | A | G | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-52+164A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20764289 | |||||||
| chr16:20764319 | C | G | 2 | a0001c0001t0001g0192a0001c0001t0005g0191 | 2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-52+194C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20764319 | |||||||
| chr16:20764541 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-52+416T>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20764541 | |||||||
| chr16:20764587 | G | T | 1 | a0002c0002t0001g0190 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-52+462G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20764587 | |||||||
| chr16:20764632 | A | G | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-52+507A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20764632 | |||||||
| chr16:20764799 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-52+674G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20764799 | |||||||
| chr16:20764936 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-52+811G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20764936 | |||||||
| chr16:20765139 | T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(90): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-52+1014T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20765139 | |||||||
| chr16:20765304 | G | A | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-52+1179G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20765304 | |||||||
| chr16:20765319 | A | G | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-52+1194A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20765319 | |||||||
| chr16:20765709 | C | T | 32 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 56 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-52+1584C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20765709 | |||||||
| chr16:20765728 | C | T | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-52+1603C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20765728 | |||||||
| chr16:20765914 | C | T | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-52+1789C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20765914 | |||||||
| chr16:20765972 | G | A | 1 | a0001c0004t0001g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-52+1847G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20765972 | |||||||
| chr16:20766305 | T | TAAGAAAT others(309): Show |
1 | a0001c0001t0001g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(318): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(310): Show |
1 | a0001c0001t0001g0037 | 2 | NA19080.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-52+2197_-52+2198i others(319): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(314): Show |
1 | a0001c0001t0001g0140 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(323): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(320): Show |
2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-52+2197_-52+2198i others(329): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(321): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(330): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(324): Show |
1 | a0001c0001t0001g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(333): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(330): Show |
1 | a0001c0001t0001g0135 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(339): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(331): Show |
6 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0132others(3): Show | 13 | HG00099.hp1 HG01109.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52+2197_-52+2198i others(340): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(332): Show |
6 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0128others(3): Show | 11 | HG00673.hp1 HG01258.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-52+2197_-52+2198i others(341): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(333): Show |
5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG03209.hp1 HG03492.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+2197_-52+2198i others(342): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(334): Show |
1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(343): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(335): Show |
1 | a0001c0001t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(344): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(337): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-52+2197_-52+2198i others(346): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(332): Show |
1 | a0001c0001t0001g0145 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(341): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(338): Show |
1 | a0001c0001t0001g0144 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(347): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(343): Show |
1 | a0001c0001t0001g0143 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(352): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766305 | T | TAAGAAAT others(344): Show |
1 | a0001c0001t0001g0142 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-52+2197_-52+2198i others(353): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20766305 | ||||||
| chr16:20766372 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-52+2247G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20766372 | |||||||
| chr16:20766610 | C | T | 33 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(30): Show | 57 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-52+2485C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20766610 | |||||||
| chr16:20766654 | A | G | 1 | a0001c0001t0002g0050 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52+2529A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20766654 | |||||||
| chr16:20767219 | CAAAAAAC others(313): Show |
C | 119 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(116): Show | 201 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-51-2748_-51-2429d others(2): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20767219 | ||||||
| chr16:20767349 | C | T | 1 | a0001c0001t0005g0191 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-51-2635C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20767349 | |||||||
| chr16:20767516 | C | CA | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(43): Show | 74 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-51-2439dupA | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20767516 | ||||||
| chr16:20767516 | C | CAA | 21 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(18): Show | 34 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-51-2440_-51-2439d others(4): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20767516 | ||||||
| chr16:20767516 | C | CAAA | 6 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0039others(3): Show | 7 | HG01081.hp2 HG02165.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-2441_-51-2439d others(5): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 20767516 | ||||||
| chr16:20767992 | A | G | 2 | a0007c0007t0001g0095a0007c0007t0001g0096 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-51-1992A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20767992 | |||||||
| chr16:20767998 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-51-1986G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20767998 | |||||||
| chr16:20768215 | A | C | 1 | a0001c0001t0001g0045 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-51-1769A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768215 | |||||||
| chr16:20768344 | A | G | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51-1640A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768344 | |||||||
| chr16:20768376 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-51-1608T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768376 | |||||||
| chr16:20768521 | G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0038 | 5 | HG00280.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-1463G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768521 | |||||||
| chr16:20768525 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-51-1459C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768525 | |||||||
| chr16:20768614 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-51-1370T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768614 | |||||||
| chr16:20768640 | A | T | 33 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(30): Show | 57 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-51-1344A>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768640 | |||||||
| chr16:20768903 | A | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0091others(3): Show | 13 | HG00140.hp2 HG01069.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51-1081A>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768903 | |||||||
| chr16:20768940 | C | T | 33 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(30): Show | 57 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-51-1044C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768940 | |||||||
| chr16:20768941 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-51-1043G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20768941 | |||||||
| chr16:20769036 | G | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0057others(5): Show | 15 | HG00140.hp2 HG01069.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51-948G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20769036 | |||||||
| chr16:20769064 | C | T | 32 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 56 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-51-920C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20769064 | |||||||
| chr16:20769478 | CTAATTGT others(5): Show |
C | 1 | a0001c0001t0001g0143 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-51-505_-51-494del others(12): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20769478 | |||||||
| chr16:20769526 | C | A | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-51-458C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20769526 | |||||||
| chr16:20769867 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01516.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-51-117C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20769867 | |||||||
| chr16:20769868 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-51-116G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20769868 | |||||||
| chr16:20769872 | C | A | 33 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(30): Show | 57 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-51-112C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20769872 | |||||||
| chr16:20769943 | A | G | 1 | a0001c0001t0001g0015 | 3 | HG01109.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-41A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 1/13 | chr16 | 20769943 | |||||||
| chr16:20770375 | T | C | 1 | a0002c0002t0001g0098 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.219+122T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770375 | |||||||
| chr16:20770426 | C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02698.hp2 HG03239.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.219+173C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770426 | |||||||
| chr16:20770438 | C | T | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219+185C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770438 | |||||||
| chr16:20770460 | C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(41): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.219+207C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770460 | |||||||
| chr16:20770530 | TA | T | 27 | a0001c0001t0001g0052a0001c0001t0001g0168a0002c0002t0001g0003others(24): Show | 46 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.219+289delA | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20770530 | ||||||
| chr16:20770537 | A | G | 25 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0017others(22): Show | 44 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.219+284A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770537 | |||||||
| chr16:20770617 | G | A | 51 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(48): Show | 88 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.219+364G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770617 | |||||||
| chr16:20770625 | T | G | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+372T>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770625 | |||||||
| chr16:20770711 | G | A | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219+458G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770711 | |||||||
| chr16:20770912 | C | A | 1 | a0002c0002t0001g0102 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.219+659C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20770912 | |||||||
| chr16:20771041 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.219+788C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771041 | |||||||
| chr16:20771051 | G | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+798G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771051 | |||||||
| chr16:20771258 | G | A | 2 | a0001c0004t0001g0006a0001c0004t0001g0059 | 8 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+1005G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771258 | |||||||
| chr16:20771296 | A | G | 1 | a0002c0002t0003g0117 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.219+1043A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771296 | |||||||
| chr16:20771364 | C | T | 1 | a0003c0003t0001g0024 | 2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.219+1111C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771364 | |||||||
| chr16:20771371 | C | CT | 52 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(49): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.219+1144dupT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20771371 | ||||||
| chr16:20771371 | C | CTT | 11 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0085others(8): Show | 16 | HG00099.hp2 HG01358.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.219+1143_219+1144d others(4): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20771371 | ||||||
| chr16:20771371 | CT | C | 30 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0022others(27): Show | 40 | HG00544.hp1 HG00558.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+1144delT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20771371 | ||||||
| chr16:20771405 | A | G | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.219+1152A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771405 | |||||||
| chr16:20771408 | G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.219+1155G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771408 | |||||||
| chr16:20771528 | C | T | 1 | a0001c0004t0001g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.219+1275C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771528 | |||||||
| chr16:20771683 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.219+1430G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771683 | |||||||
| chr16:20771717 | A | G | 51 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(48): Show | 88 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.219+1464A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771717 | |||||||
| chr16:20771803 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.219+1550G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771803 | |||||||
| chr16:20771826 | T | C | 12 | a0001c0004t0001g0006a0001c0004t0001g0055a0001c0004t0001g0059others(9): Show | 23 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.219+1573T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771826 | |||||||
| chr16:20771956 | A | G | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+1703A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20771956 | |||||||
| chr16:20772111 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.219+1858G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772111 | |||||||
| chr16:20772393 | A | T | 2 | a0007c0007t0001g0095a0007c0007t0001g0096 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.219+2140A>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772393 | |||||||
| chr16:20772397 | T | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 12 | HG01358.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+2144T>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772397 | |||||||
| chr16:20772415 | TA | T | 32 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 56 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.219+2168delA | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20772415 | ||||||
| chr16:20772473 | C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.219+2220C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772473 | |||||||
| chr16:20772527 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.219+2274G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772527 | |||||||
| chr16:20772644 | C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(36): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.219+2391C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772644 | |||||||
| chr16:20772694 | A | C | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+2441A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772694 | |||||||
| chr16:20772716 | A | G | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219+2463A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772716 | |||||||
| chr16:20772824 | G | A | 29 | a0001c0001t0001g0085a0001c0004t0001g0006a0001c0004t0001g0059others(26): Show | 54 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.219+2571G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772824 | |||||||
| chr16:20772967 | C | CA | 6 | a0001c0001t0001g0071a0001c0001t0001g0118a0001c0001t0001g0130others(3): Show | 7 | HG01175.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.219+2730dupA | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20772967 | ||||||
| chr16:20772973 | A | G | 1 | a0002c0002t0001g0098 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.219+2720A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20772973 | |||||||
| chr16:20773171 | A | C | 12 | a0001c0004t0001g0006a0001c0004t0001g0055a0001c0004t0001g0059others(9): Show | 23 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.220-2668A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20773171 | |||||||
| chr16:20773483 | G | A | 8 | a0003c0003t0001g0011a0003c0003t0001g0023a0003c0003t0001g0024others(5): Show | 13 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.220-2356G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20773483 | |||||||
| chr16:20773549 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.220-2290T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20773549 | |||||||
| chr16:20773849 | A | G | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.220-1990A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20773849 | |||||||
| chr16:20773974 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.220-1865A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20773974 | |||||||
| chr16:20774217 | T | C | 1 | a0001c0004t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.220-1622T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774217 | |||||||
| chr16:20774239 | C | CT | 34 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0031others(31): Show | 55 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.220-1579dupT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20774239 | ||||||
| chr16:20774239 | C | CTT | 5 | a0001c0001t0001g0101a0002c0002t0001g0017a0003c0003t0001g0065others(2): Show | 7 | HG02080.hp1 HG03704.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-1580_220-1579d others(4): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20774239 | ||||||
| chr16:20774239 | CT | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0122a0001c0001t0001g0169others(5): Show | 15 | HG02257.hp1 HG02572.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.220-1579delT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20774239 | ||||||
| chr16:20774265 | C | T | 30 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0018others(27): Show | 43 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.220-1574C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774265 | |||||||
| chr16:20774277 | C | G | 10 | a0001c0004t0001g0055a0001c0004t0001g0064a0003c0003t0001g0011others(7): Show | 15 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.220-1562C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774277 | |||||||
| chr16:20774279 | G | GT | 3 | a0004c0005t0001g0048a0004c0005t0001g0182a0004c0005t0001g0186 | 4 | HG02622.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-1559dupT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 20774279 | ||||||
| chr16:20774281 | C | G | 3 | a0004c0005t0001g0048a0004c0005t0001g0182a0004c0005t0001g0186 | 4 | HG02622.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-1558C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774281 | |||||||
| chr16:20774282 | A | C | 3 | a0004c0005t0001g0048a0004c0005t0001g0182a0004c0005t0001g0186 | 4 | HG02622.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-1557A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774282 | |||||||
| chr16:20774394 | T | C | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.220-1445T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774394 | |||||||
| chr16:20774463 | G | A | 2 | a0003c0003t0001g0023a0003c0003t0001g0060 | 3 | HG02615.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-1376G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774463 | |||||||
| chr16:20774533 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.220-1306G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774533 | |||||||
| chr16:20774603 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-1236G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774603 | |||||||
| chr16:20774666 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.220-1173T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774666 | |||||||
| chr16:20774689 | G | T | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.220-1150G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774689 | |||||||
| chr16:20774895 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.220-944G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20774895 | |||||||
| chr16:20775026 | T | C | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.220-813T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20775026 | |||||||
| chr16:20775094 | G | A | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.220-745G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20775094 | |||||||
| chr16:20775095 | C | T | 12 | a0001c0004t0001g0006a0001c0004t0001g0055a0001c0004t0001g0059others(9): Show | 23 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.220-744C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20775095 | |||||||
| chr16:20775221 | G | A | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.220-618G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20775221 | |||||||
| chr16:20775423 | G | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 5 | HG01168.hp2 HG01169.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-416G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20775423 | |||||||
| chr16:20775440 | G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0090 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.220-399G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 2/13 | chr16 | 20775440 | |||||||
| chr16:20776145 | G | A | 14 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0037others(11): Show | 18 | HG00673.hp1 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.430+96G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20776145 | |||||||
| chr16:20776190 | C | A | 30 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0018others(27): Show | 43 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.430+141C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20776190 | |||||||
| chr16:20776190 | C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | NA18964.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.430+141C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20776190 | |||||||
| chr16:20776448 | G | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.430+399G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20776448 | |||||||
| chr16:20776623 | A | G | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.430+574A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20776623 | |||||||
| chr16:20776716 | T | A | 2 | a0007c0007t0001g0095a0007c0007t0001g0096 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.431-657T>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20776716 | |||||||
| chr16:20776862 | T | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(92): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.431-511T>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20776862 | |||||||
| chr16:20777240 | T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0056 | 3 | NA18990.hp1 NA19075.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.431-133T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20777240 | |||||||
| chr16:20777267 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.431-106C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 3/13 | chr16 | 20777267 | |||||||
| chr16:20777583 | G | A | 2 | a0007c0007t0001g0095a0007c0007t0001g0096 | 2 | HG03704.hp2 HG03927.hp2 |
splice_region_variant&intron_variant | LOW | c.638+3G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20777583 | |||||||
| chr16:20777623 | A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0146 | 8 | HG01099.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.638+43A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20777623 | |||||||
| chr16:20777638 | G | T | 2 | a0003c0003t0001g0061a0003c0003t0001g0063 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.638+58G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20777638 | |||||||
| chr16:20777649 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.638+69C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20777649 | |||||||
| chr16:20777661 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.638+81G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20777661 | |||||||
| chr16:20777769 | T | G | 1 | a0002c0002t0001g0034 | 2 | HG00673.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.638+189T>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20777769 | |||||||
| chr16:20777955 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.638+375C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20777955 | |||||||
| chr16:20778013 | G | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+433G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778013 | |||||||
| chr16:20778058 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.638+478A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778058 | |||||||
| chr16:20778226 | T | C | 12 | a0001c0004t0001g0006a0001c0004t0001g0055a0001c0004t0001g0059others(9): Show | 23 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.638+646T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778226 | |||||||
| chr16:20778278 | G | A | 1 | a0001c0001t0001g0043 | 2 | NA19007.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.638+698G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778278 | |||||||
| chr16:20778346 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.638+766T>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778346 | |||||||
| chr16:20778391 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.638+811C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778391 | |||||||
| chr16:20778426 | G | T | 2 | a0007c0007t0001g0095a0007c0007t0001g0096 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.638+846G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778426 | |||||||
| chr16:20778757 | C | CT | 9 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0057others(6): Show | 16 | HG00140.hp2 HG01069.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.638+1189dupT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20778757 | ||||||
| chr16:20778773 | C | T | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+1193C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778773 | |||||||
| chr16:20778837 | A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(92): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.638+1257A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778837 | |||||||
| chr16:20778983 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.638+1403C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778983 | |||||||
| chr16:20778993 | T | C | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+1413T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20778993 | |||||||
| chr16:20779021 | G | A | 8 | a0003c0003t0001g0011a0003c0003t0001g0023a0003c0003t0001g0024others(5): Show | 13 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.638+1441G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779021 | |||||||
| chr16:20779042 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.638+1462C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779042 | |||||||
| chr16:20779043 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01358.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.638+1463G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779043 | |||||||
| chr16:20779093 | T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0073others(2): Show | 7 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.638+1513T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779093 | |||||||
| chr16:20779285 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.639-1429T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779285 | |||||||
| chr16:20779366 | A | G | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.639-1348A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779366 | |||||||
| chr16:20779399 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.639-1315G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779399 | |||||||
| chr16:20779425 | C | CA | 37 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(34): Show | 82 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.639-1275dupA | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20779425 | ||||||
| chr16:20779425 | CA | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(87): Show | 163 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.639-1275delA | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20779425 | ||||||
| chr16:20779761 | G | A | 2 | a0001c0004t0001g0006a0001c0004t0001g0059 | 8 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.639-953G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779761 | |||||||
| chr16:20779771 | CT | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0027others(42): Show | 66 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.639-925delT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20779771 | ||||||
| chr16:20779771 | CTT | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(31): Show | 58 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.639-926_639-925del others(2): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 20779771 | ||||||
| chr16:20779834 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.639-880C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20779834 | |||||||
| chr16:20780043 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.639-671G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20780043 | |||||||
| chr16:20780121 | G | A | 1 | a0004c0005t0001g0048 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.639-593G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20780121 | |||||||
| chr16:20780135 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.639-579A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20780135 | |||||||
| chr16:20780184 | C | A | 49 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(46): Show | 86 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.639-530C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20780184 | |||||||
| chr16:20780267 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.639-447C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20780267 | |||||||
| chr16:20780604 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.639-110C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 4/13 | chr16 | 20780604 | |||||||
| chr16:20780866 | T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(116): Show | 201 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.782+9T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 5/13 | chr16 | 20780866 | |||||||
| chr16:20781259 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.939+129A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/13 | chr16 | 20781259 | |||||||
| chr16:20781480 | C | T | 2 | a0007c0007t0001g0095a0007c0007t0001g0096 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.940-228C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/13 | chr16 | 20781480 | |||||||
| chr16:20781481 | G | A | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.940-227G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/13 | chr16 | 20781481 | |||||||
| chr16:20781518 | A | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 6 | HG00735.hp2 HG01074.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-190A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/13 | chr16 | 20781518 | |||||||
| chr16:20781563 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.940-145C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/13 | chr16 | 20781563 | |||||||
| chr16:20781592 | A | C | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 59 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.940-116A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 6/13 | chr16 | 20781592 | |||||||
| chr16:20781807 | A | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(31): Show | 58 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1019+20A>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20781807 | |||||||
| chr16:20781913 | C | T | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1019+126C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20781913 | |||||||
| chr16:20781969 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1019+182C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20781969 | |||||||
| chr16:20782147 | C | A | 1 | a0001c0001t0005g0191 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1019+360C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782147 | |||||||
| chr16:20782212 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1019+425C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782212 | |||||||
| chr16:20782299 | A | G | 1 | a0002c0002t0001g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1019+512A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782299 | |||||||
| chr16:20782346 | C | T | 12 | a0001c0004t0001g0006a0001c0004t0001g0055a0001c0004t0001g0059others(9): Show | 23 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1019+559C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782346 | |||||||
| chr16:20782348 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1019+561A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782348 | |||||||
| chr16:20782421 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1019+634A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782421 | |||||||
| chr16:20782444 | C | T | 1 | a0002c0002t0001g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1019+657C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782444 | |||||||
| chr16:20782550 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1019+763C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782550 | |||||||
| chr16:20782900 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1019+1113T>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20782900 | |||||||
| chr16:20783103 | T | G | 1 | a0001c0004t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1019+1316T>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20783103 | |||||||
| chr16:20783105 | C | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0183 | 3 | HG02056.hp2 HG02523.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1019+1318C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20783105 | |||||||
| chr16:20783146 | C | T | 1 | a0001c0004t0001g0006 | 7 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1019+1359C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20783146 | |||||||
| chr16:20783177 | A | T | 32 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 56 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1019+1390A>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20783177 | |||||||
| chr16:20783435 | T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0073others(2): Show | 7 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020-1549T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20783435 | |||||||
| chr16:20783626 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1020-1358G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20783626 | |||||||
| chr16:20783661 | A | G | 42 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(39): Show | 67 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1020-1323A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20783661 | |||||||
| chr16:20783812 | A | AT | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(182): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1020-1159dupT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 20783812 | ||||||
| chr16:20783964 | C | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0185 | 4 | HG02559.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020-1020C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20783964 | |||||||
| chr16:20784109 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1020-875C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20784109 | |||||||
| chr16:20784793 | C | T | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1020-191C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20784793 | |||||||
| chr16:20784967 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1020-17T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 7/13 | chr16 | 20784967 | |||||||
| chr16:20785140 | T | C | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1143+33T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 8/13 | chr16 | 20785140 | |||||||
| chr16:20785186 | T | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(41): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1143+79T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 8/13 | chr16 | 20785186 | |||||||
| chr16:20785568 | GAATGAAA others(11): Show |
G | 1 | a0002c0002t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1144-478_1144-461d others(20): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 20785568 | ||||||
| chr16:20786169 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1224+11C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786169 | |||||||
| chr16:20786219 | C | T | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1224+61C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786219 | |||||||
| chr16:20786440 | G | A | 2 | a0001c0004t0001g0006a0001c0004t0001g0059 | 8 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1224+282G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786440 | |||||||
| chr16:20786448 | A | C | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1224+290A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786448 | |||||||
| chr16:20786452 | G | A | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1224+294G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786452 | |||||||
| chr16:20786527 | TA | T | 3 | a0004c0005t0001g0048a0004c0005t0001g0182a0004c0005t0001g0186 | 4 | HG02622.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+375delA | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 20786527 | ||||||
| chr16:20786553 | C | T | 14 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0037others(11): Show | 18 | HG00673.hp1 HG01975.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1224+395C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786553 | |||||||
| chr16:20786651 | C | G | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1224+493C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786651 | |||||||
| chr16:20786704 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1224+546A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786704 | |||||||
| chr16:20786770 | C | G | 2 | a0001c0004t0001g0055a0001c0004t0001g0064 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1224+612C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786770 | |||||||
| chr16:20786890 | T | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(41): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1224+732T>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786890 | |||||||
| chr16:20786920 | G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(116): Show | 201 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1224+762G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20786920 | |||||||
| chr16:20787049 | G | C | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1224+891G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787049 | |||||||
| chr16:20787055 | C | G | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1224+897C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787055 | |||||||
| chr16:20787124 | G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(41): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1224+966G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787124 | |||||||
| chr16:20787428 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1224+1270A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787428 | |||||||
| chr16:20787509 | C | T | 1 | a0001c0001t0001g0049 | 2 | NA18612.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1224+1351C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787509 | |||||||
| chr16:20787604 | A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(92): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1224+1446A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787604 | |||||||
| chr16:20787746 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1224+1588C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787746 | |||||||
| chr16:20787775 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1224+1617G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787775 | |||||||
| chr16:20787948 | A | C | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1224+1790A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787948 | |||||||
| chr16:20787972 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1224+1814C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20787972 | |||||||
| chr16:20788040 | A | G | 1 | a0001c0004t0001g0006 | 7 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1224+1882A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788040 | |||||||
| chr16:20788108 | A | T | 3 | a0001c0001t0001g0160a0007c0007t0001g0095a0007c0007t0001g0096 | 3 | HG03704.hp2 HG03927.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1224+1950A>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788108 | |||||||
| chr16:20788112 | T | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0154a0001c0004t0001g0006others(1): Show | 12 | HG00544.hp2 HG00735.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1224+1954T>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788112 | |||||||
| chr16:20788131 | T | C | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1224+1973T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788131 | |||||||
| chr16:20788257 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1224+2099C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788257 | |||||||
| chr16:20788344 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1224+2186C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788344 | |||||||
| chr16:20788412 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1225-2175G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788412 | |||||||
| chr16:20788484 | T | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(90): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1225-2103T>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788484 | |||||||
| chr16:20788485 | T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(90): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1225-2102T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788485 | |||||||
| chr16:20788528 | T | C | 2 | a0007c0007t0001g0095a0007c0007t0001g0096 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1225-2059T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788528 | |||||||
| chr16:20788637 | C | A | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1225-1950C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788637 | |||||||
| chr16:20788897 | A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0159 | 4 | HG00423.hp2 HG02083.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-1690A>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788897 | |||||||
| chr16:20788907 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1225-1680G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20788907 | |||||||
| chr16:20789248 | T | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0046others(22): Show | 33 | HG00544.hp1 HG00558.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.1225-1339T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20789248 | |||||||
| chr16:20789594 | A | G | 46 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1225-993A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20789594 | |||||||
| chr16:20789611 | G | T | 1 | a0002c0002t0001g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1225-976G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20789611 | |||||||
| chr16:20789684 | C | CT | 11 | a0001c0001t0001g0080a0001c0001t0001g0125a0001c0001t0001g0129others(8): Show | 11 | HG00609.hp1 HG00741.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1225-884dupT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 20789684 | ||||||
| chr16:20789684 | CT | C | 8 | a0001c0001t0001g0046a0001c0001t0001g0084a0001c0001t0001g0091others(5): Show | 9 | HG00140.hp2 HG01167.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-884delT | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 20789684 | ||||||
| chr16:20789688 | T | C | 1 | a0001c0016t0001g0068 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1225-899T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20789688 | |||||||
| chr16:20789689 | T | C | 3 | a0002c0002t0001g0107a0002c0002t0001g0109a0002c0002t0001g0111 | 3 | HG00423.hp1 HG00438.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1225-898T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20789689 | |||||||
| chr16:20789921 | G | A | 1 | a0001c0001t0001g0049 | 2 | NA18612.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1225-666G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20789921 | |||||||
| chr16:20790020 | C | T | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1225-567C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20790020 | |||||||
| chr16:20790146 | TA | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0018others(30): Show | 46 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1225-438delA | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 20790146 | ||||||
| chr16:20790265 | T | C | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1225-322T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20790265 | |||||||
| chr16:20790345 | G | C | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1225-242G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20790345 | |||||||
| chr16:20790386 | G | C | 8 | a0003c0003t0001g0011a0003c0003t0001g0023a0003c0003t0001g0024others(5): Show | 13 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1225-201G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 9/13 | chr16 | 20790386 | |||||||
| chr16:20790802 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1326+114T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 10/13 | chr16 | 20790802 | |||||||
| chr16:20790850 | C | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0018others(30): Show | 46 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1326+162C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 10/13 | chr16 | 20790850 | |||||||
| chr16:20790912 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1326+224C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 10/13 | chr16 | 20790912 | |||||||
| chr16:20791639 | A | G | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1327-363A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 10/13 | chr16 | 20791639 | |||||||
| chr16:20791655 | G | A | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1327-347G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 10/13 | chr16 | 20791655 | |||||||
| chr16:20791847 | G | A | 2 | a0001c0004t0001g0006a0001c0004t0001g0059 | 8 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1327-155G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 10/13 | chr16 | 20791847 | |||||||
| chr16:20792413 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1554+78C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20792413 | |||||||
| chr16:20792597 | A | G | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1554+262A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20792597 | |||||||
| chr16:20792630 | G | A | 3 | a0002c0002t0001g0104a0002c0002t0001g0106a0002c0002t0001g0112 | 3 | HG03688.hp1 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1554+295G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20792630 | |||||||
| chr16:20792776 | C | A | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1554+441C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20792776 | |||||||
| chr16:20792776 | C | G | 1 | a0001c0001t0001g0038 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1554+441C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20792776 | |||||||
| chr16:20792949 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1554+614G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20792949 | |||||||
| chr16:20792976 | T | C | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1554+641T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20792976 | |||||||
| chr16:20793161 | T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(90): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1554+826T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793161 | |||||||
| chr16:20793220 | G | A | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1554+885G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793220 | |||||||
| chr16:20793281 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1554+946C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793281 | |||||||
| chr16:20793464 | G | A | 3 | a0001c0001t0002g0040a0001c0001t0002g0050a0001c0001t0002g0148 | 5 | HG02622.hp2 HG02723.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1554+1129G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793464 | |||||||
| chr16:20793465 | C | T | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1554+1130C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793465 | |||||||
| chr16:20793470 | A | AAAAAATA others(5): Show |
1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1554+1147_1554+115 others(16): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20793470 | ||||||
| chr16:20793497 | TTAAGG | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(31): Show | 58 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1554+1166_1554+117 others(9): Show |
ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 20793497 | ||||||
| chr16:20793544 | C | A | 4 | a0001c0001t0001g0031a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 5 | HG01168.hp2 HG01169.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1554+1209C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793544 | |||||||
| chr16:20793658 | T | C | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1554+1323T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793658 | |||||||
| chr16:20793683 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1554+1348G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793683 | |||||||
| chr16:20793744 | A | G | 2 | a0007c0007t0001g0095a0007c0007t0001g0096 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1554+1409A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793744 | |||||||
| chr16:20793774 | C | T | 1 | a0002c0002t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1554+1439C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793774 | |||||||
| chr16:20793787 | C | T | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1554+1452C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793787 | |||||||
| chr16:20793927 | C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 6 | HG00735.hp2 HG01074.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1554+1592C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20793927 | |||||||
| chr16:20794048 | G | C | 4 | a0001c0001t0001g0176a0004c0005t0001g0048a0004c0005t0001g0182others(1): Show | 5 | HG02622.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1554+1713G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20794048 | |||||||
| chr16:20794424 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1555-1946G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20794424 | |||||||
| chr16:20794542 | G | A | 1 | a0010c0011t0001g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1555-1828G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20794542 | |||||||
| chr16:20794587 | C | T | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1555-1783C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20794587 | |||||||
| chr16:20794779 | C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0082 | 2 | HG01255.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1555-1591C>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20794779 | |||||||
| chr16:20794850 | A | C | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1555-1520A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20794850 | |||||||
| chr16:20795330 | T | C | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1555-1040T>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20795330 | |||||||
| chr16:20795443 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1555-927C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20795443 | |||||||
| chr16:20795474 | C | G | 1 | a0001c0008t0001g0030 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1555-896C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20795474 | |||||||
| chr16:20795543 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1555-827G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20795543 | |||||||
| chr16:20795583 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1555-787A>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20795583 | |||||||
| chr16:20795669 | C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0156a0001c0001t0001g0163others(1): Show | 11 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1555-701C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20795669 | |||||||
| chr16:20795670 | G | A | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1555-700G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20795670 | |||||||
| chr16:20795766 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1555-604G>C | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20795766 | |||||||
| chr16:20796127 | A | G | 1 | a0006c0009t0001g0051 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1555-243A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20796127 | |||||||
| chr16:20796132 | C | T | 2 | a0003c0003t0001g0061a0003c0003t0001g0063 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1555-238C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20796132 | |||||||
| chr16:20796363 | A | G | 1 | a0001c0001t0001g0039 | 2 | NA18967.hp2 NA19055.hp2 |
splice_region_variant&intron_variant | LOW | c.1555-7A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 12/13 | chr16 | 20796363 | |||||||
| chr16:20796509 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1674+20C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 13/13 | chr16 | 20796509 | |||||||
| chr16:20796595 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1674+106G>A | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 13/13 | chr16 | 20796595 | |||||||
| chr16:20796691 | G | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0134 | 2 | NA19005.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1675-195G>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 13/13 | chr16 | 20796691 | |||||||
| chr16:20796698 | A | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0018others(30): Show | 46 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1675-188A>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 13/13 | chr16 | 20796698 | |||||||
| chr16:20796722 | C | G | 1 | a0001c0012t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1675-164C>G | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 13/13 | chr16 | 20796722 | |||||||
| chr16:20796871 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1675-15C>T | ACSM3 | ENSG00000005187.12 | transcript | ENST00000289416.10 | protein_coding | 13/13 | chr16 | 20796871 |