Search by Gene
| Item | Value |
|---|---|
| geneid | 51703 |
| ensemblid | ENSG00000197142.11 |
| hgncid | 16526 |
| symbol | ACSL5 |
| name | acyl-CoA synthetase long chain family member 5 |
| refseq_nuc | NM_203379.2 |
| refseq_prot | NP_976313.1 |
| ensembl_nuc | ENST00000354655.9 |
| ensembl_prot | ENSP00000346680.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 112374116 |
| end | 112428376 |
| strand | + |
| ver | v1.2 |
| region | chr10:112374116-112428376 |
| region5000 | chr10:112369116-112433376 |
| regionname0 | ACSL5_chr10_112374116_112428376 |
| regionname5000 | ACSL5_chr10_112369116_112433376 |
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 | 683 | 327 | 86 | 57 | 129 | 10 | 43 | ACSL5_chr10_112369116_112433376 | ACSL5 | MLFIF others(678): Show |
chr10 | 112369116 | 112433376 |
| a0002 | 0/0 | 683 | 27 | 1 | 5 | 19 | 2 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | MLFIF others(678): Show |
chr10 | 112369116 | 112433376 |
| a0003 | 0/0 | 683 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | MLFIF others(678): Show |
chr10 | 112369116 | 112433376 |
| a0004 | 0/0 | 683 | 2 | 1 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | MLFIF others(678): Show |
chr10 | 112369116 | 112433376 |
| a0005 | 0/0 | 683 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | MLFIF others(678): Show |
chr10 | 112369116 | 112433376 |
| a0006 | 0/0 | 683 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | MLFIF others(678): Show |
chr10 | 112369116 | 112433376 |
| a0007 | 0/0 | 683 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | MLFIF others(678): Show |
chr10 | 112369116 | 112433376 |
| a0008 | 0/0 | 683 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | MLFIF others(678): Show |
chr10 | 112369116 | 112433376 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2049 | 319 | 82 | 56 | 128 | 9 | 42 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0001c0003 | 0/0 | 2049 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0001c0005 | 0/0 | 2049 | 2 | 0 | 1 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0001c0010 | 0/0 | 2049 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0001c0012 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0002c0002 | 0/0 | 2049 | 27 | 1 | 5 | 19 | 2 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0003c0004 | 0/0 | 2049 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0004c0006 | 0/0 | 2049 | 2 | 1 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0005c0009 | 0/0 | 2049 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0006c0007 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0007c0011 | 0/0 | 2049 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 | ||
| a0008c0008 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ATGCT others(2044): Show |
chr10 | 112369116 | 112433376 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3253 | 167 | 42 | 29 | 63 | 7 | 25 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0001t0002 | 0/1 | 3253 | 134 | 35 | 25 | 54 | 2 | 17 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0001t0003 | 0/0 | 3253 | 12 | 0 | 1 | 11 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0001t0004 | 0/0 | 3253 | 3 | 3 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0001t0005 | 0/0 | 3253 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0001t0006 | 0/0 | 3253 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0001t0007 | 0/0 | 3253 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0003t0002 | 0/0 | 3253 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0005t0001 | 0/0 | 3253 | 2 | 0 | 1 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0010t0001 | 0/0 | 3253 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0001c0012t0001 | 0/0 | 3253 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0002c0002t0001 | 0/0 | 3253 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0002c0002t0003 | 0/0 | 3253 | 26 | 1 | 5 | 18 | 2 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0003c0004t0002 | 0/0 | 3253 | 4 | 4 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0004c0006t0001 | 0/0 | 3253 | 2 | 1 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0005c0009t0001 | 0/0 | 3253 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0006c0007t0002 | 0/0 | 3253 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0007c0011t0001 | 0/0 | 3253 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| a0008c0008t0002 | 0/0 | 3253 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | ACTCT others(3248): Show |
chr10 | 112369116 | 112433376 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0003t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0003t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0005t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0001c0012t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0003c0004t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0003c0004t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0003c0004t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0003c0004t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0004c0006t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0004c0006t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0005c0009t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0006c0007t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0007c0011t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| a0008c0008t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | GBR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | GBR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00140 | hp1 | a0001 | c0005 | t0001 | g0262 | EUR | GBR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00323 | hp2 | a0002 | c0002 | t0003 | g0125 | EUR | FIN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | CHS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0120 | EAS | CHS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | CHS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | CHS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0118 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01081 | hp1 | a0002 | c0002 | t0003 | g0123 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0344 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0336 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0119 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01255 | hp1 | a0005 | c0009 | t0001 | g0134 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01361 | hp1 | a0001 | c0005 | t0001 | g0252 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01433 | hp1 | a0004 | c0006 | t0001 | g0166 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | IBS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | IBS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0130 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0343 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0126 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0128 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02135 | hp1 | a0001 | c0012 | t0001 | g0272 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CDX | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0159 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02451 | hp2 | a0004 | c0006 | t0001 | g0186 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0323 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0340 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02896 | hp1 | a0003 | c0004 | t0002 | g0017 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03130 | hp1 | a0003 | c0004 | t0002 | g0319 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0339 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0258 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03453 | hp1 | a0006 | c0007 | t0002 | g0303 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03579 | hp1 | a0003 | c0004 | t0002 | g0337 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | STU | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | STU | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG04199 | hp2 | a0007 | c0011 | t0001 | g0179 | SAS | STU | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | STU | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | STU | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG04228 | hp2 | a0001 | c0010 | t0001 | g0096 | SAS | STU | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | YRI | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | YRI | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18906 | hp1 | a0008 | c0008 | t0002 | g0017 | AFR | YRI | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0338 | AFR | YRI | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18939 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18953 | hp2 | a0002 | c0002 | t0003 | g0157 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18961 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18962 | hp1 | a0002 | c0002 | t0003 | g0129 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18965 | hp2 | a0002 | c0002 | t0003 | g0131 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0161 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0164 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19012 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | LWK | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | LWK | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19066 | hp2 | a0002 | c0002 | t0003 | g0160 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0143 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19082 | hp1 | a0002 | c0002 | t0003 | g0158 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0162 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0257 | AFR | YRI | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0341 | AFR | ASW | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ASW | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA20805 | hp2 | a0002 | c0002 | t0003 | g0124 | EUR | TSI | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0142 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0342 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | ACB | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG06807 | hp1 | a0003 | c0004 | t0002 | g0320 | AFR | USA | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | USA | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | USA | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | LWK | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0111 | REF | REF | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0139 | REF | REF | ACSL5_chr10_112369116_112433376 | ACSL5 | chr10 | 112369116 | 112433376 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:112394996 | T | C | 1 | a0006 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.50T>C | p.Leu17Ser | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/21 | 233/3253 | 50/2052 | 17/683 | chr10 | 112394996 | |||
| chr10:112409518 | A | G | 1 | a0002 | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
missense_variant | MODERATE | c.544A>G | p.Met182Val | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 7/21 | 727/3253 | 544/2052 | 182/683 | chr10 | 112409518 | |||
| chr10:112410599 | G | A | 1 | a0008 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.760G>A | p.Asp254Asn | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 9/21 | 943/3253 | 760/2052 | 254/683 | chr10 | 112410599 | |||
| chr10:112413225 | G | A | 1 | a0005 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1001G>A | p.Arg334Gln | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/21 | 1184/3253 | 1001/2052 | 334/683 | chr10 | 112413225 | |||
| chr10:112413273 | C | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1049C>T | p.Ala350Val | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/21 | 1232/3253 | 1049/2052 | 350/683 | chr10 | 112413273 | |||
| chr10:112417858 | G | A | 1 | a0004 | 2 | HG01433.hp1 HG02451.hp2 |
missense_variant | MODERATE | c.1231G>A | p.Gly411Arg | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/21 | 1414/3253 | 1231/2052 | 411/683 | chr10 | 112417858 | |||
| chr10:112422015 | A | G | 2 | a0003a0008 | 5 | HG02896.hp1 HG03130.hp1 HG03579.hp1 others(2): Show |
missense_variant | MODERATE | c.1456A>G | p.Thr486Ala | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 16/21 | 1639/3253 | 1456/2052 | 486/683 | chr10 | 112422015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:112394994 | G | A | 1 | a0001c0005 | 2 | HG00140.hp1 HG01361.hp1 |
synonymous_variant | LOW | c.48G>A | p.Ala16Ala | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/21 | 231/3253 | 48/2052 | 16/683 | chr10 | 112394994 | |||
| chr10:112395057 | C | T | 1 | a0002c0002 | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
synonymous_variant | LOW | c.111C>T | p.Pro37Pro | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/21 | 294/3253 | 111/2052 | 37/683 | chr10 | 112395057 | |||
| chr10:112408502 | C | T | 1 | a0001c0012 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.513C>T | p.Ile171Ile | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/21 | 696/3253 | 513/2052 | 171/683 | chr10 | 112408502 | |||
| chr10:112416935 | G | A | 1 | a0001c0003 | 4 | HG02559.hp2 HG03225.hp1 NA19030.hp1 others(1): Show |
synonymous_variant | LOW | c.1131G>A | p.Leu377Leu | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/21 | 1314/3253 | 1131/2052 | 377/683 | chr10 | 112416935 | |||
| chr10:112425424 | T | C | 1 | a0001c0010 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.1680T>C | p.Asn560Asn | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 18/21 | 1863/3253 | 1680/2052 | 560/683 | chr10 | 112425424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:112374168 | G | A | 1 | a0001c0001t0005 | 1 | HG01123.hp1 | 5_prime_UTR_variant | MODIFIER | c.-131G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/21 | 20779 | chr10 | 112374168 | ||||||
| chr10:112374237 | C | A | 1 | a0001c0001t0006 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/21 | 20710 | chr10 | 112374237 | ||||||
| chr10:112427906 | C | T | 1 | a0001c0001t0007 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*548C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 21/21 | 548 | chr10 | 112427906 | ||||||
| chr10:112428029 | T | C | 5 | a0001c0001t0002a0001c0003t0002a0003c0004t0002others(2): Show | 143 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*671T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 21/21 | 671 | chr10 | 112428029 | ||||||
| chr10:112428069 | T | A | 3 | a0001c0001t0003a0001c0001t0007a0002c0002t0003 | 39 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*711T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 21/21 | 711 | chr10 | 112428069 | ||||||
| chr10:112428173 | G | T | 1 | a0001c0001t0004 | 3 | HG02258.hp1 HG03486.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*815G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 21/21 | 815 | chr10 | 112428173 | ||||||
| chr10:112428328 | T | C | 3 | a0001c0001t0003a0001c0001t0007a0002c0002t0003 | 39 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*970T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 21/21 | 970 | chr10 | 112428328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:112374372 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-30+103T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112374372 | |||||||
| chr10:112374399 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-30+130A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112374399 | |||||||
| chr10:112374455 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30+186T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112374455 | |||||||
| chr10:112374517 | A | T | 150 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.-30+248A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112374517 | |||||||
| chr10:112374558 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30+289A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112374558 | |||||||
| chr10:112374719 | T | A | 1 | a0001c0001t0002g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-30+450T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112374719 | |||||||
| chr10:112374792 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-30+523C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112374792 | |||||||
| chr10:112375040 | G | A | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30+771G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375040 | |||||||
| chr10:112375052 | T | TA | 93 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0029others(90): Show | 94 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-30+793dupA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112375052 | ||||||
| chr10:112375063 | G | A | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.-30+794G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375063 | |||||||
| chr10:112375063 | G | T | 71 | a0001c0001t0001g0165a0001c0001t0002g0001a0001c0001t0002g0020others(68): Show | 72 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30+794G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375063 | |||||||
| chr10:112375064 | A | AT | 46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(43): Show | 50 | HG00738.hp2 HG01070.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.-30+795_-30+796ins others(1): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375064 | |||||||
| chr10:112375255 | C | T | 78 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(75): Show | 79 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-30+986C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375255 | |||||||
| chr10:112375297 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30+1028G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375297 | |||||||
| chr10:112375323 | ATGTCCAA others(33): Show |
A | 10 | a0002c0002t0003g0003a0002c0002t0003g0004a0002c0002t0003g0157others(7): Show | 12 | HG02293.hp2 NA18948.hp1 NA18953.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30+1058_-30+1097d others(42): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112375323 | ||||||
| chr10:112375421 | A | G | 3 | a0001c0001t0001g0345a0001c0001t0002g0343a0001c0001t0002g0344 | 3 | HG01099.hp1 HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-30+1152A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375421 | |||||||
| chr10:112375502 | G | A | 5 | a0001c0001t0002g0020a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG01243.hp2 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+1233G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375502 | |||||||
| chr10:112375585 | G | A | 1 | a0004c0006t0001g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-30+1316G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375585 | |||||||
| chr10:112375694 | C | T | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30+1425C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375694 | |||||||
| chr10:112375794 | G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-30+1525G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375794 | |||||||
| chr10:112375931 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30+1662G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375931 | |||||||
| chr10:112375993 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-30+1724C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112375993 | |||||||
| chr10:112376019 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-30+1750A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376019 | |||||||
| chr10:112376220 | C | T | 5 | a0001c0001t0002g0338a0001c0001t0002g0339a0001c0001t0002g0340others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+1951C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376220 | |||||||
| chr10:112376438 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30+2169C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376438 | |||||||
| chr10:112376496 | G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+2227G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376496 | |||||||
| chr10:112376591 | G | C | 147 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(144): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-30+2322G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376591 | |||||||
| chr10:112376645 | G | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.-30+2376G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376645 | |||||||
| chr10:112376701 | G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-30+2432G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376701 | |||||||
| chr10:112376777 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-30+2508G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376777 | |||||||
| chr10:112376924 | A | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+2655A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376924 | |||||||
| chr10:112376972 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-30+2703A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112376972 | |||||||
| chr10:112376973 | GTAAGCAC others(36): Show |
G | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(143): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.-30+2731_-30+2773d others(45): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112376973 | ||||||
| chr10:112376973 | GTAAGCAC others(79): Show |
G | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+2731_-30+2816d others(88): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112376973 | ||||||
| chr10:112376987 | GGGACTCT others(35): Show |
G | 1 | a0001c0001t0001g0295 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-30+2721_-30+2762d others(44): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112376987 | ||||||
| chr10:112377000 | T | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0027others(167): Show | 177 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.-30+2731T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112377000 | |||||||
| chr10:112377086 | C | T | 1 | a0001c0001t0006g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-30+2817C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112377086 | |||||||
| chr10:112377087 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-30+2818G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112377087 | |||||||
| chr10:112377094 | C | T | 1 | a0004c0006t0001g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-30+2825C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112377094 | |||||||
| chr10:112377565 | AC | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0002g0023others(6): Show | 9 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+3297delC | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112377565 | |||||||
| chr10:112377650 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-30+3381T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112377650 | |||||||
| chr10:112377909 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-30+3640A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112377909 | |||||||
| chr10:112378227 | G | GT | 17 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0041others(14): Show | 17 | HG00609.hp1 HG01109.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-30+3989dupT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112378227 | ||||||
| chr10:112378227 | GT | G | 48 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0127others(45): Show | 49 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-30+3989delT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112378227 | ||||||
| chr10:112378227 | GTT | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0043others(102): Show | 109 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-30+3988_-30+3989d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112378227 | ||||||
| chr10:112378227 | GTTT | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(76): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-30+3987_-30+3989d others(5): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112378227 | ||||||
| chr10:112378227 | GTTTT | G | 68 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 73 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-30+3986_-30+3989d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112378227 | ||||||
| chr10:112378227 | GTTTTTTT others(7): Show |
G | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01978.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+3976_-30+3989d others(16): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112378227 | ||||||
| chr10:112378227 | GTTTTTTT others(8): Show |
G | 2 | a0002c0002t0003g0118a0002c0002t0003g0119 | 2 | HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-30+3975_-30+3989d others(17): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112378227 | ||||||
| chr10:112378267 | C | G | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30+3998C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112378267 | |||||||
| chr10:112378270 | A | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(309): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-30+4001A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112378270 | |||||||
| chr10:112378485 | T | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(144): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-30+4216T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112378485 | |||||||
| chr10:112378663 | C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+4394C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112378663 | |||||||
| chr10:112378809 | C | G | 1 | a0001c0001t0002g0084 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-30+4540C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112378809 | |||||||
| chr10:112378895 | TTGGAAGG others(12): Show |
T | 28 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0117others(25): Show | 31 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-30+4629_-30+4647d others(21): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112378895 | ||||||
| chr10:112378914 | G | A | 147 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(144): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-30+4645G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112378914 | |||||||
| chr10:112379256 | C | T | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(143): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.-30+4987C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112379256 | |||||||
| chr10:112379266 | G | A | 32 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0298others(29): Show | 34 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-30+4997G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112379266 | |||||||
| chr10:112379414 | G | GA | 276 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(273): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.-30+5159dupA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112379414 | ||||||
| chr10:112379414 | G | GAA | 30 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0117others(27): Show | 33 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.-30+5158_-30+5159d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112379414 | ||||||
| chr10:112379489 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-30+5220G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112379489 | |||||||
| chr10:112379572 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+5303A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112379572 | |||||||
| chr10:112379614 | C | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA19006.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-30+5345C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112379614 | |||||||
| chr10:112379913 | A | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+5644A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112379913 | |||||||
| chr10:112380007 | A | G | 3 | a0001c0001t0001g0022a0001c0001t0004g0032a0001c0001t0004g0033 | 3 | HG02258.hp1 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-30+5738A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112380007 | |||||||
| chr10:112380120 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-30+5851G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112380120 | |||||||
| chr10:112380138 | G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(309): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-30+5869G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112380138 | |||||||
| chr10:112380507 | G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+6238G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112380507 | |||||||
| chr10:112380640 | G | A | 1 | a0002c0002t0003g0128 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-30+6371G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112380640 | |||||||
| chr10:112380819 | G | A | 1 | a0001c0001t0002g0336 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-30+6550G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112380819 | |||||||
| chr10:112380846 | A | G | 67 | a0001c0001t0001g0165a0001c0001t0002g0001a0001c0001t0002g0045others(64): Show | 68 | HG00099.hp2 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-30+6577A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112380846 | |||||||
| chr10:112381033 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-30+6764G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381033 | |||||||
| chr10:112381242 | G | A | 1 | a0001c0001t0002g0001 | 2 | HG01934.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-30+6973G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381242 | |||||||
| chr10:112381345 | G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0117others(26): Show | 32 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-30+7076G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381345 | |||||||
| chr10:112381441 | G | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+7172G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381441 | |||||||
| chr10:112381487 | T | G | 129 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(126): Show | 132 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-30+7218T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381487 | |||||||
| chr10:112381520 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+7251C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381520 | |||||||
| chr10:112381521 | C | A | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+7252C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381521 | |||||||
| chr10:112381523 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+7254G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381523 | |||||||
| chr10:112381524 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+7255A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381524 | |||||||
| chr10:112381525 | T | G | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+7256T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381525 | |||||||
| chr10:112381665 | CA | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.-30+7415delA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112381665 | ||||||
| chr10:112381665 | CAA | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0167others(38): Show | 45 | HG01433.hp1 HG01884.hp1 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.-30+7414_-30+7415d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112381665 | ||||||
| chr10:112381665 | CAAAAAA | C | 13 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG00738.hp2 HG01070.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.-30+7410_-30+7415d others(8): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112381665 | ||||||
| chr10:112381795 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-30+7526A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381795 | |||||||
| chr10:112381859 | C | G | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30+7590C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381859 | |||||||
| chr10:112381870 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-30+7601G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381870 | |||||||
| chr10:112381918 | T | TTAAAAAA others(42): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 6 | NA18959.hp1 NA18983.hp1 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+7649_-30+7650i others(51): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112381918 | |||||||
| chr10:112382010 | C | T | 2 | a0001c0001t0002g0333a0001c0001t0002g0334 | 2 | HG00544.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-30+7741C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382010 | |||||||
| chr10:112382023 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-30+7754G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382023 | |||||||
| chr10:112382064 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30+7795C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382064 | |||||||
| chr10:112382238 | T | A | 1 | a0001c0001t0002g0088 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-30+7969T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382238 | |||||||
| chr10:112382302 | T | C | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-30+8033T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382302 | |||||||
| chr10:112382346 | G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0117others(25): Show | 31 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-30+8077G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382346 | |||||||
| chr10:112382552 | C | T | 1 | a0002c0002t0003g0161 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-30+8283C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382552 | |||||||
| chr10:112382588 | T | G | 3 | a0001c0001t0001g0022a0001c0001t0004g0032a0001c0001t0004g0033 | 3 | HG02258.hp1 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-30+8319T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382588 | |||||||
| chr10:112382641 | T | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.-30+8372T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382641 | |||||||
| chr10:112382918 | C | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+8649C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382918 | |||||||
| chr10:112382938 | C | T | 4 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+8669C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112382938 | |||||||
| chr10:112383049 | G | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-30+8780G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383049 | |||||||
| chr10:112383114 | TAAAAACA | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0253others(7): Show | 10 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+8863_-30+8869d others(9): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112383114 | ||||||
| chr10:112383184 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-30+8915C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383184 | |||||||
| chr10:112383292 | G | A | 3 | a0001c0001t0002g0302a0001c0001t0002g0321a0006c0007t0002g0303 | 3 | HG02109.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-30+9023G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383292 | |||||||
| chr10:112383314 | A | G | 1 | a0001c0001t0003g0332 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-30+9045A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383314 | |||||||
| chr10:112383423 | G | A | 1 | a0004c0006t0001g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-30+9154G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383423 | |||||||
| chr10:112383466 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-30+9197A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383466 | |||||||
| chr10:112383670 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-30+9401C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383670 | |||||||
| chr10:112383812 | C | CT | 176 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0022others(173): Show | 183 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.-30+9552dupT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112383812 | ||||||
| chr10:112383812 | C | CTT | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-30+9551_-30+9552d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112383812 | ||||||
| chr10:112383828 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-30+9559G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383828 | |||||||
| chr10:112383920 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-30+9651C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383920 | |||||||
| chr10:112383984 | A | G | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-30+9715A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112383984 | |||||||
| chr10:112384081 | G | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-30+9812G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384081 | |||||||
| chr10:112384197 | C | A | 1 | a0001c0001t0002g0085 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-30+9928C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384197 | |||||||
| chr10:112384203 | AC | A | 3 | a0002c0002t0003g0120a0002c0002t0003g0121a0002c0002t0003g0128 | 3 | HG00544.hp2 HG02129.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.-30+9935delC | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384203 | |||||||
| chr10:112384304 | GTT | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-30+10036_-30+1003 others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384304 | |||||||
| chr10:112384375 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-30+10106A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384375 | |||||||
| chr10:112384388 | A | G | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30+10119A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384388 | |||||||
| chr10:112384454 | G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-30+10185G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384454 | |||||||
| chr10:112384507 | G | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0002g0023others(6): Show | 9 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+10238G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384507 | |||||||
| chr10:112384660 | G | A | 3 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0001t0002g0305 | 3 | NA18944.hp2 NA18954.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-29-10258G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384660 | |||||||
| chr10:112384708 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-29-10210G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384708 | |||||||
| chr10:112384794 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-29-10124G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384794 | |||||||
| chr10:112384813 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-29-10105G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384813 | |||||||
| chr10:112384973 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-29-9945C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112384973 | |||||||
| chr10:112385134 | C | T | 1 | a0001c0001t0002g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-29-9784C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112385134 | |||||||
| chr10:112385135 | G | C | 1 | a0001c0001t0002g0089 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-29-9783G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112385135 | |||||||
| chr10:112385194 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-29-9724G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112385194 | |||||||
| chr10:112385286 | A | G | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(97): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.-29-9632A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112385286 | |||||||
| chr10:112385444 | A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-9474A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112385444 | |||||||
| chr10:112385486 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-29-9432C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112385486 | |||||||
| chr10:112385541 | A | G | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01891.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-9377A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112385541 | |||||||
| chr10:112385595 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-29-9323T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112385595 | |||||||
| chr10:112386047 | T | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0004g0032others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-8871T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386047 | |||||||
| chr10:112386181 | C | CT | 12 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0141others(9): Show | 12 | HG00609.hp1 HG01175.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29-8707dupT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112386181 | ||||||
| chr10:112386181 | C | CTT | 6 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0002g0028others(3): Show | 6 | HG00639.hp2 HG00642.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-8708_-29-8707d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112386181 | ||||||
| chr10:112386181 | CT | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0034others(128): Show | 137 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(134): Show |
intron_variant | MODIFIER | c.-29-8707delT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112386181 | ||||||
| chr10:112386181 | CTT | C | 9 | a0001c0001t0002g0036a0001c0001t0002g0049a0001c0001t0002g0338others(6): Show | 9 | HG02818.hp2 HG03195.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-8708_-29-8707d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112386181 | ||||||
| chr10:112386181 | CTTTTTTT others(2): Show |
C | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(132): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.-29-8715_-29-8707d others(11): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112386181 | ||||||
| chr10:112386181 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0174a0001c0001t0001g0189a0001c0001t0001g0210others(4): Show | 7 | HG00558.hp1 HG01517.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-8716_-29-8707d others(12): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112386181 | ||||||
| chr10:112386181 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0008 | 2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-29-8721_-29-8707d others(17): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112386181 | ||||||
| chr10:112386332 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-29-8586T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386332 | |||||||
| chr10:112386459 | G | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-29-8459G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386459 | |||||||
| chr10:112386571 | A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0184a0001c0001t0001g0185 | 4 | HG02280.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8347A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386571 | |||||||
| chr10:112386572 | T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0184a0001c0001t0001g0185 | 4 | HG02280.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-8346T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386572 | |||||||
| chr10:112386687 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-29-8231C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386687 | |||||||
| chr10:112386744 | T | G | 130 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(127): Show | 134 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-29-8174T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386744 | |||||||
| chr10:112386745 | T | C | 130 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(127): Show | 134 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-29-8173T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386745 | |||||||
| chr10:112386880 | T | C | 1 | a0001c0001t0006g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29-8038T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386880 | |||||||
| chr10:112386987 | C | T | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-29-7931C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112386987 | |||||||
| chr10:112387011 | T | C | 4 | a0001c0001t0001g0165a0001c0001t0002g0050a0001c0001t0002g0051others(1): Show | 4 | HG01358.hp2 HG01433.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-7907T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112387011 | |||||||
| chr10:112387276 | T | C | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-29-7642T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112387276 | |||||||
| chr10:112387525 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-29-7393G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112387525 | |||||||
| chr10:112387899 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-29-7019G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112387899 | |||||||
| chr10:112387936 | C | CT | 132 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(129): Show | 136 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.-29-6963dupT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112387936 | ||||||
| chr10:112387936 | C | CTT | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.-29-6964_-29-6963d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112387936 | ||||||
| chr10:112387936 | C | CTTT | 6 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0281others(3): Show | 6 | HG01361.hp1 HG02055.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-6965_-29-6963d others(5): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112387936 | ||||||
| chr10:112387984 | G | T | 4 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0248others(1): Show | 4 | HG02523.hp1 NA18953.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-6934G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112387984 | |||||||
| chr10:112388039 | A | G | 8 | a0001c0001t0001g0014a0001c0001t0001g0208a0001c0001t0001g0209others(5): Show | 9 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-6879A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388039 | |||||||
| chr10:112388064 | G | A | 5 | a0003c0004t0002g0017a0003c0004t0002g0319a0003c0004t0002g0320others(2): Show | 5 | HG02896.hp1 HG03130.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-6854G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388064 | |||||||
| chr10:112388132 | G | C | 1 | a0001c0001t0002g0314 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-29-6786G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388132 | |||||||
| chr10:112388139 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-29-6779C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388139 | |||||||
| chr10:112388230 | G | A | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-29-6688G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388230 | |||||||
| chr10:112388260 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-29-6658C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388260 | |||||||
| chr10:112388315 | C | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0198a0001c0001t0002g0199 | 4 | HG02615.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-6603C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388315 | |||||||
| chr10:112388367 | C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0197a0001c0001t0001g0205 | 3 | HG02738.hp1 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-29-6551C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388367 | |||||||
| chr10:112388383 | C | T | 2 | a0002c0002t0003g0130a0002c0002t0003g0131 | 2 | HG01928.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-29-6535C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388383 | |||||||
| chr10:112388611 | G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0347 | 2 | HG01175.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-29-6307G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388611 | |||||||
| chr10:112388621 | A | G | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-29-6297A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388621 | |||||||
| chr10:112388726 | C | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-6192C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388726 | |||||||
| chr10:112388931 | C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-29-5987C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112388931 | |||||||
| chr10:112389069 | T | A | 1 | a0001c0001t0002g0325 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-29-5849T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112389069 | |||||||
| chr10:112389375 | G | C | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-29-5543G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112389375 | |||||||
| chr10:112389465 | C | A | 3 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0084 | 3 | NA18612.hp2 NA19064.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-29-5453C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112389465 | |||||||
| chr10:112389547 | T | C | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-29-5371T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112389547 | |||||||
| chr10:112389721 | C | A | 150 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(147): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-29-5197C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112389721 | |||||||
| chr10:112389868 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-29-5050A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112389868 | |||||||
| chr10:112390102 | AAG | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-29-4812_-29-4811d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112390102 | ||||||
| chr10:112390655 | A | AATAG | 39 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0127others(36): Show | 39 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.-29-4221_-29-4218d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112390655 | ||||||
| chr10:112390655 | A | AATAGATA others(1): Show |
8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG01515.hp2 HG01517.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29-4225_-29-4218d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112390655 | ||||||
| chr10:112390655 | AATAG | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(118): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-29-4221_-29-4218d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112390655 | ||||||
| chr10:112390655 | AATAGATA others(1): Show |
A | 53 | a0001c0001t0001g0022a0001c0001t0001g0173a0001c0001t0001g0217others(50): Show | 55 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-29-4225_-29-4218d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112390655 | ||||||
| chr10:112390655 | AATAGATA others(5): Show |
A | 40 | a0001c0001t0001g0009a0001c0001t0001g0216a0001c0001t0002g0015others(37): Show | 43 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-29-4229_-29-4218d others(14): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112390655 | ||||||
| chr10:112390841 | A | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-4077A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112390841 | |||||||
| chr10:112391024 | C | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0167others(40): Show | 46 | HG00738.hp2 HG01070.hp2 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.-29-3894C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391024 | |||||||
| chr10:112391025 | G | A | 1 | a0001c0001t0002g0343 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-29-3893G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391025 | |||||||
| chr10:112391043 | G | A | 5 | a0001c0001t0002g0338a0001c0001t0002g0339a0001c0001t0002g0340others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-3875G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391043 | |||||||
| chr10:112391135 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-29-3783T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391135 | |||||||
| chr10:112391238 | G | A | 1 | a0002c0002t0003g0004 | 2 | NA18948.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-29-3680G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391238 | |||||||
| chr10:112391284 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-29-3634C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391284 | |||||||
| chr10:112391318 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-29-3600C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391318 | |||||||
| chr10:112391368 | C | CA | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(250): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-29-3536dupA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112391368 | ||||||
| chr10:112391368 | C | CAA | 6 | a0001c0001t0001g0214a0001c0001t0001g0281a0001c0001t0002g0057others(3): Show | 6 | HG01981.hp1 HG04228.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-3537_-29-3536d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112391368 | ||||||
| chr10:112391436 | T | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0002g0023others(6): Show | 9 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-3482T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391436 | |||||||
| chr10:112391437 | G | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01891.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-3481G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391437 | |||||||
| chr10:112391689 | T | A | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-29-3229T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391689 | |||||||
| chr10:112391904 | T | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.-29-3014T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391904 | |||||||
| chr10:112391917 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-29-3001G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391917 | |||||||
| chr10:112391999 | T | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.-29-2919T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112391999 | |||||||
| chr10:112392198 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-29-2720G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392198 | |||||||
| chr10:112392252 | ACTTGAGC others(128): Show |
A | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.-29-2557_-29-2423d others(2): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112392252 | ||||||
| chr10:112392364 | T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 59 | HG00738.hp2 HG01070.hp2 HG01175.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-2554T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392364 | |||||||
| chr10:112392456 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-29-2462A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392456 | |||||||
| chr10:112392461 | G | T | 1 | a0001c0001t0002g0007 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-29-2457G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392461 | |||||||
| chr10:112392469 | C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.-29-2449C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392469 | |||||||
| chr10:112392666 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-29-2252G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392666 | |||||||
| chr10:112392670 | G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-2248G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392670 | |||||||
| chr10:112392740 | C | CA | 126 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(123): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-29-2161dupA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112392740 | ||||||
| chr10:112392905 | A | G | 9 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0002g0023others(6): Show | 9 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-2013A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392905 | |||||||
| chr10:112392907 | C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0206 | 3 | NA18977.hp2 NA18999.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-29-2011C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392907 | |||||||
| chr10:112392908 | G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-2010G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392908 | |||||||
| chr10:112392931 | A | C | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-29-1987A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112392931 | |||||||
| chr10:112393033 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-29-1885T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393033 | |||||||
| chr10:112393038 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-29-1880C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393038 | |||||||
| chr10:112393054 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-29-1864C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393054 | |||||||
| chr10:112393178 | A | G | 11 | a0001c0001t0001g0014a0001c0001t0001g0208a0001c0001t0001g0209others(8): Show | 12 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29-1740A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393178 | |||||||
| chr10:112393314 | G | A | 3 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0084 | 3 | NA18612.hp2 NA19064.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-29-1604G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393314 | |||||||
| chr10:112393398 | G | A | 5 | a0001c0001t0002g0338a0001c0001t0002g0339a0001c0001t0002g0340others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-1520G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393398 | |||||||
| chr10:112393441 | C | T | 25 | a0002c0002t0001g0122a0002c0002t0003g0003a0002c0002t0003g0004others(22): Show | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-29-1477C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393441 | |||||||
| chr10:112393731 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-29-1187C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393731 | |||||||
| chr10:112393792 | G | A | 2 | a0001c0001t0001g0040a0001c0001t0003g0019 | 2 | HG00639.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-1126G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393792 | |||||||
| chr10:112393875 | A | G | 331 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(328): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-29-1043A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393875 | |||||||
| chr10:112393940 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-29-978C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112393940 | |||||||
| chr10:112394051 | GC | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-29-865delC | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 112394051 | ||||||
| chr10:112394355 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-29-563C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394355 | |||||||
| chr10:112394419 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-29-499A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394419 | |||||||
| chr10:112394453 | T | G | 1 | a0001c0001t0002g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-29-465T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394453 | |||||||
| chr10:112394463 | T | C | 1 | a0001c0001t0002g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-29-455T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394463 | |||||||
| chr10:112394593 | G | C | 1 | a0001c0001t0001g0293 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-29-325G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394593 | |||||||
| chr10:112394703 | A | G | 321 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-29-215A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394703 | |||||||
| chr10:112394801 | C | T | 1 | a0002c0002t0003g0160 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-29-117C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394801 | |||||||
| chr10:112394805 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-29-113C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394805 | |||||||
| chr10:112394809 | C | T | 1 | a0001c0001t0002g0338 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-29-109C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394809 | |||||||
| chr10:112394811 | T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-107T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 1/20 | chr10 | 112394811 | |||||||
| chr10:112395139 | CCTCAAAC others(10): Show |
C | 1 | a0002c0002t0003g0158 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.156+38_156+54delCT others(15): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112395139 | |||||||
| chr10:112395311 | C | T | 6 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | HG00639.hp2 HG01891.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+209C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112395311 | |||||||
| chr10:112395462 | C | T | 1 | a0001c0001t0006g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.156+360C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112395462 | |||||||
| chr10:112395828 | C | T | 25 | a0002c0002t0001g0122a0002c0002t0003g0003a0002c0002t0003g0004others(22): Show | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.156+726C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112395828 | |||||||
| chr10:112395925 | A | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+823A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112395925 | |||||||
| chr10:112395933 | T | C | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.156+831T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112395933 | |||||||
| chr10:112396069 | T | C | 321 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.156+967T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112396069 | |||||||
| chr10:112396442 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.156+1340A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112396442 | |||||||
| chr10:112396497 | C | T | 8 | a0001c0001t0002g0020a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG00642.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+1395C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112396497 | |||||||
| chr10:112396686 | T | TCA | 5 | a0001c0001t0001g0022a0001c0001t0002g0015a0001c0001t0002g0300others(2): Show | 6 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+1604_156+1605d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 112396686 | ||||||
| chr10:112396694 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.156+1592A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112396694 | |||||||
| chr10:112396702 | A | G | 9 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0002g0023others(6): Show | 9 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.156+1600A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112396702 | |||||||
| chr10:112396949 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.156+1847G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112396949 | |||||||
| chr10:112396983 | G | T | 75 | a0001c0001t0001g0165a0001c0001t0002g0001a0001c0001t0002g0020others(72): Show | 76 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.156+1881G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112396983 | |||||||
| chr10:112397005 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-1896A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112397005 | |||||||
| chr10:112397076 | G | T | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01891.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-1825G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112397076 | |||||||
| chr10:112397169 | CTT | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.157-1716_157-1715d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 112397169 | ||||||
| chr10:112397243 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.157-1658C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112397243 | |||||||
| chr10:112397255 | C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-1646C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112397255 | |||||||
| chr10:112397412 | C | T | 7 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287others(4): Show | 7 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-1489C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112397412 | |||||||
| chr10:112397525 | G | A | 2 | a0001c0001t0001g0147a0005c0009t0001g0134 | 2 | HG01255.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.157-1376G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112397525 | |||||||
| chr10:112397660 | A | G | 24 | a0001c0001t0001g0011a0001c0001t0001g0210a0001c0001t0001g0211others(21): Show | 25 | HG00558.hp1 HG00609.hp2 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.157-1241A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112397660 | |||||||
| chr10:112397858 | A | G | 1 | a0004c0006t0001g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.157-1043A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112397858 | |||||||
| chr10:112398026 | TACAGATC others(331): Show |
T | 316 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(313): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.157-857_157-520del | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 112398026 | ||||||
| chr10:112398041 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0004g0033 | 3 | HG02965.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.157-830_157-818del others(13): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 112398041 | ||||||
| chr10:112398041 | CTTTTTTT others(7): Show |
C | 6 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0002g0030others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-831_157-818del others(14): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 112398041 | ||||||
| chr10:112398041 | CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0001g0027a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG02818.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-832_157-818del others(15): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 112398041 | ||||||
| chr10:112398041 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0146 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.157-835_157-818del others(18): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 112398041 | ||||||
| chr10:112398685 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.157-216G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112398685 | |||||||
| chr10:112398809 | G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0210a0001c0001t0001g0276others(4): Show | 8 | HG00558.hp1 HG00609.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-92G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 2/20 | chr10 | 112398809 | |||||||
| chr10:112399150 | A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.265+141A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112399150 | |||||||
| chr10:112399473 | C | G | 1 | a0001c0001t0006g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.265+464C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112399473 | |||||||
| chr10:112399504 | G | A | 1 | a0001c0001t0002g0304 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.265+495G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112399504 | |||||||
| chr10:112399694 | G | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.265+685G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112399694 | |||||||
| chr10:112399979 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.265+970C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112399979 | |||||||
| chr10:112400002 | C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.265+993C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400002 | |||||||
| chr10:112400054 | G | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.265+1045G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400054 | |||||||
| chr10:112400235 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.265+1226G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400235 | |||||||
| chr10:112400382 | A | AT | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.265+1382dupT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112400382 | ||||||
| chr10:112400406 | C | CT | 141 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(138): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.265+1418dupT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112400406 | ||||||
| chr10:112400406 | C | CTT | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(51): Show | 58 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.265+1417_265+1418d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112400406 | ||||||
| chr10:112400406 | CTTTTTTT others(1): Show |
C | 25 | a0002c0002t0001g0122a0002c0002t0003g0003a0002c0002t0003g0004others(22): Show | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.265+1411_265+1418d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112400406 | ||||||
| chr10:112400410 | T | TC | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG00558.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+1401_265+1402i others(3): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400410 | |||||||
| chr10:112400411 | T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0007g0021 | 3 | HG01884.hp2 HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.265+1402T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400411 | |||||||
| chr10:112400412 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.265+1403T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400412 | |||||||
| chr10:112400592 | A | G | 6 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | HG00639.hp2 HG01891.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1583A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400592 | |||||||
| chr10:112400629 | A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.265+1620A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400629 | |||||||
| chr10:112400726 | T | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.265+1717T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400726 | |||||||
| chr10:112400765 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.265+1756G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400765 | |||||||
| chr10:112400937 | G | C | 1 | a0001c0001t0002g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.265+1928G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400937 | |||||||
| chr10:112400953 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.265+1944G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400953 | |||||||
| chr10:112400955 | G | C | 25 | a0002c0002t0001g0122a0002c0002t0003g0003a0002c0002t0003g0004others(22): Show | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.265+1946G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112400955 | |||||||
| chr10:112401030 | C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0167others(38): Show | 44 | HG00738.hp2 HG01070.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.265+2021C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401030 | |||||||
| chr10:112401031 | G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+2022G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401031 | |||||||
| chr10:112401104 | C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.265+2095C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401104 | |||||||
| chr10:112401116 | T | C | 13 | a0001c0001t0002g0302a0001c0001t0002g0321a0001c0001t0002g0338others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+2107T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401116 | |||||||
| chr10:112401129 | T | C | 1 | a0001c0001t0006g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.265+2120T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401129 | |||||||
| chr10:112401131 | G | T | 13 | a0001c0001t0002g0302a0001c0001t0002g0321a0001c0001t0002g0338others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+2122G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401131 | |||||||
| chr10:112401230 | A | C | 1 | a0001c0001t0001g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.265+2221A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401230 | |||||||
| chr10:112401308 | T | C | 1 | a0004c0006t0001g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.265+2299T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401308 | |||||||
| chr10:112401398 | G | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.265+2389G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401398 | |||||||
| chr10:112401565 | G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+2556G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401565 | |||||||
| chr10:112401695 | T | C | 5 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG02155.hp1 HG03834.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+2686T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401695 | |||||||
| chr10:112401698 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.265+2689C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401698 | |||||||
| chr10:112401705 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.265+2696A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401705 | |||||||
| chr10:112401761 | T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01884.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.266-2750T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401761 | |||||||
| chr10:112401784 | T | TTCTC | 8 | a0001c0001t0001g0042a0001c0001t0002g0026a0001c0001t0002g0030others(5): Show | 8 | HG00099.hp2 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-2725_266-2722d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401784 | ||||||
| chr10:112401786 | C | CTCTT | 13 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0141others(10): Show | 13 | HG01175.hp2 HG01884.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.266-2672_266-2669d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401786 | ||||||
| chr10:112401786 | C | CTCTTTCT others(1): Show |
4 | a0001c0001t0001g0178a0001c0001t0001g0251a0001c0001t0002g0269others(1): Show | 4 | HG01123.hp1 HG03130.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-2676_266-2669d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401786 | ||||||
| chr10:112401786 | C | CTCTTTCT others(5): Show |
1 | a0001c0001t0001g0146 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.266-2680_266-2669d others(14): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401786 | ||||||
| chr10:112401786 | CTCTT | C | 23 | a0001c0001t0001g0034a0001c0001t0001g0116a0001c0001t0001g0140others(20): Show | 23 | HG01109.hp1 HG01243.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.266-2672_266-2669d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401786 | ||||||
| chr10:112401786 | CTCTTTCT others(1): Show |
C | 9 | a0001c0001t0001g0117a0001c0001t0001g0173a0001c0001t0001g0201others(6): Show | 9 | HG01433.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.266-2676_266-2669d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401786 | ||||||
| chr10:112401786 | CTCTTTCT others(5): Show |
C | 2 | a0001c0001t0001g0022a0001c0001t0001g0181 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.266-2680_266-2669d others(14): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401786 | ||||||
| chr10:112401786 | CTCTTTCT others(9): Show |
C | 2 | a0001c0001t0002g0007a0001c0001t0002g0198 | 3 | HG02615.hp1 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.266-2684_266-2669d others(18): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401786 | ||||||
| chr10:112401786 | CTCTTTCT others(13): Show |
C | 2 | a0001c0001t0001g0002a0001c0001t0002g0199 | 3 | HG02809.hp1 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.266-2688_266-2669d others(22): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401786 | ||||||
| chr10:112401787 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.266-2724T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401787 | |||||||
| chr10:112401790 | T | C | 122 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0044others(119): Show | 127 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.266-2721T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401790 | |||||||
| chr10:112401794 | T | C | 10 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0024others(7): Show | 10 | HG01243.hp2 HG01515.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.266-2717T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401794 | |||||||
| chr10:112401795 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.266-2716T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401795 | |||||||
| chr10:112401798 | T | C | 5 | a0001c0001t0002g0047a0001c0001t0002g0285a0001c0001t0002g0286others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-2713T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401798 | |||||||
| chr10:112401823 | TCTTTCTT others(17): Show |
T | 1 | a0001c0001t0002g0307 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.266-2684_266-2661d others(26): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401823 | ||||||
| chr10:112401827 | TCTTTCTT others(9): Show |
T | 5 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0076others(2): Show | 5 | HG00558.hp2 HG03209.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-2680_266-2665d others(18): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401827 | ||||||
| chr10:112401827 | TCTTTCTT others(13): Show |
T | 10 | a0001c0001t0001g0029a0001c0001t0001g0209a0001c0001t0001g0226others(7): Show | 10 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.266-2680_266-2661d others(22): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401827 | ||||||
| chr10:112401829 | TTTCTTTC others(12): Show |
T | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.266-2678_266-2660d others(21): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401829 | ||||||
| chr10:112401831 | TCTTTCTT others(5): Show |
T | 26 | a0001c0001t0002g0016a0001c0001t0002g0054a0001c0001t0002g0059others(23): Show | 26 | HG00642.hp1 HG01192.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.266-2676_266-2665d others(14): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401831 | ||||||
| chr10:112401831 | TCTTTCTT others(9): Show |
T | 16 | a0001c0001t0001g0010a0001c0001t0001g0113a0001c0001t0001g0114others(13): Show | 17 | HG01074.hp1 HG02055.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.266-2676_266-2661d others(18): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401831 | ||||||
| chr10:112401835 | TCTTTCTT others(1): Show |
T | 43 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0044others(40): Show | 46 | HG00544.hp1 HG00597.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.266-2672_266-2665d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401835 | ||||||
| chr10:112401835 | TCTTTCTT others(5): Show |
T | 16 | a0001c0001t0001g0011a0001c0001t0001g0137a0001c0001t0001g0149others(13): Show | 17 | HG00741.hp1 HG01081.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.266-2672_266-2661d others(14): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401835 | ||||||
| chr10:112401839 | T | C | 20 | a0001c0001t0001g0156a0001c0001t0001g0171a0001c0001t0001g0183others(17): Show | 20 | HG01109.hp1 HG01515.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.266-2672T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401839 | |||||||
| chr10:112401839 | T | TCTTC | 6 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0180others(3): Show | 7 | HG01070.hp2 HG01192.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-2656_266-2653d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401839 | ||||||
| chr10:112401839 | T | TCTTTCTT others(1): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0195a0001c0001t0001g0347 | 4 | HG00738.hp2 HG01175.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-2669_266-2668i others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401839 | ||||||
| chr10:112401839 | T | TCTTTCTT others(5): Show |
2 | a0001c0001t0001g0189a0007c0011t0001g0179 | 2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.266-2669_266-2668i others(14): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401839 | ||||||
| chr10:112401839 | T | TCTTTCTT others(9): Show |
1 | a0001c0001t0001g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.266-2669_266-2668i others(18): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401839 | ||||||
| chr10:112401839 | TCTTC | T | 56 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0133others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.266-2656_266-2653d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401839 | ||||||
| chr10:112401839 | TCTTCCTT others(1): Show |
T | 39 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0027others(36): Show | 39 | HG00140.hp1 HG00558.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.266-2660_266-2653d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401839 | ||||||
| chr10:112401843 | C | T | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0018others(46): Show | 50 | HG00099.hp2 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.266-2668C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401843 | |||||||
| chr10:112401847 | C | T | 63 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0018others(60): Show | 64 | HG00609.hp1 HG00609.hp2 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.266-2664C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401847 | |||||||
| chr10:112401851 | CCTTCCTT others(1): Show |
C | 2 | a0001c0001t0002g0015a0001c0001t0003g0019 | 3 | HG00639.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.266-2656_266-2649d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401851 | ||||||
| chr10:112401859 | T | C | 23 | a0001c0001t0001g0165a0001c0001t0002g0023a0001c0001t0002g0024others(20): Show | 24 | HG01358.hp2 HG01433.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.266-2652T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401859 | |||||||
| chr10:112401947 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.266-2564T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112401947 | |||||||
| chr10:112401947 | T | TTC | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.266-2543_266-2542d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401947 | ||||||
| chr10:112401947 | T | TTCTC | 7 | a0001c0001t0001g0137a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG01361.hp2 HG01934.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-2545_266-2542d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr10 | 112401947 | ||||||
| chr10:112402113 | A | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG01496.hp2 HG02004.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.266-2398A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112402113 | |||||||
| chr10:112402461 | C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0265 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.266-2050C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112402461 | |||||||
| chr10:112402690 | C | T | 345 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(342): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.266-1821C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112402690 | |||||||
| chr10:112402702 | T | C | 2 | a0001c0001t0002g0058a0001c0001t0002g0069 | 2 | HG02717.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.266-1809T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112402702 | |||||||
| chr10:112403022 | C | A | 1 | a0001c0001t0001g0293 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.266-1489C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403022 | |||||||
| chr10:112403122 | C | T | 2 | a0002c0002t0003g0130a0002c0002t0003g0131 | 2 | HG01928.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.266-1389C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403122 | |||||||
| chr10:112403365 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.266-1146G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403365 | |||||||
| chr10:112403524 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.266-987G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403524 | |||||||
| chr10:112403562 | A | G | 25 | a0002c0002t0001g0122a0002c0002t0003g0003a0002c0002t0003g0004others(22): Show | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.266-949A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403562 | |||||||
| chr10:112403646 | T | G | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.266-865T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403646 | |||||||
| chr10:112403689 | T | G | 1 | a0001c0001t0002g0326 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.266-822T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403689 | |||||||
| chr10:112403715 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.266-796T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403715 | |||||||
| chr10:112403757 | C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(99): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.266-754C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403757 | |||||||
| chr10:112403769 | G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-742G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403769 | |||||||
| chr10:112403794 | A | T | 1 | a0001c0001t0002g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.266-717A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112403794 | |||||||
| chr10:112404115 | G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0149 | 2 | HG02080.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.266-396G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112404115 | |||||||
| chr10:112404210 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.266-301G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112404210 | |||||||
| chr10:112404275 | C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0029 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.266-236C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112404275 | |||||||
| chr10:112404318 | C | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.266-193C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112404318 | |||||||
| chr10:112404388 | T | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.266-123T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 3/20 | chr10 | 112404388 | |||||||
| chr10:112404828 | A | G | 1 | a0002c0002t0003g0125 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.432+22A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112404828 | |||||||
| chr10:112404876 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.432+70C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112404876 | |||||||
| chr10:112404945 | C | G | 4 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0028others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+139C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112404945 | |||||||
| chr10:112404971 | A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.432+165A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112404971 | |||||||
| chr10:112405041 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.432+235A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112405041 | |||||||
| chr10:112405286 | A | G | 3 | a0001c0003t0002g0013a0001c0003t0002g0257a0001c0003t0002g0258 | 4 | HG02559.hp2 HG03225.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+480A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112405286 | |||||||
| chr10:112405565 | A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.432+759A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112405565 | |||||||
| chr10:112405636 | C | G | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.432+830C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112405636 | |||||||
| chr10:112405718 | C | G | 1 | a0001c0001t0002g0053 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.432+912C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112405718 | |||||||
| chr10:112405806 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.432+1000C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112405806 | |||||||
| chr10:112405842 | G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG01884.hp2 HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.432+1036G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112405842 | |||||||
| chr10:112405858 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.432+1052T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112405858 | |||||||
| chr10:112406024 | A | G | 327 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(324): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.432+1218A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406024 | |||||||
| chr10:112406042 | C | G | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.432+1236C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406042 | |||||||
| chr10:112406218 | A | T | 67 | a0001c0001t0001g0165a0001c0001t0002g0001a0001c0001t0002g0045others(64): Show | 68 | HG00099.hp2 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.432+1412A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406218 | |||||||
| chr10:112406378 | C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0167others(38): Show | 44 | HG00738.hp2 HG01070.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.432+1572C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406378 | |||||||
| chr10:112406458 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.432+1652A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406458 | |||||||
| chr10:112406533 | A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.432+1727A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406533 | |||||||
| chr10:112406623 | T | C | 337 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.433-1799T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406623 | |||||||
| chr10:112406715 | G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-1707G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406715 | |||||||
| chr10:112406735 | C | T | 1 | a0002c0002t0003g0121 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.433-1687C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406735 | |||||||
| chr10:112406822 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.433-1600G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406822 | |||||||
| chr10:112406896 | T | C | 10 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0112others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.433-1526T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406896 | |||||||
| chr10:112406990 | C | T | 142 | a0001c0001t0001g0165a0001c0001t0002g0001a0001c0001t0002g0015others(139): Show | 146 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.433-1432C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112406990 | |||||||
| chr10:112407158 | G | C | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.433-1264G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112407158 | |||||||
| chr10:112407295 | C | T | 1 | a0004c0006t0001g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.433-1127C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112407295 | |||||||
| chr10:112407458 | G | A | 25 | a0002c0002t0001g0122a0002c0002t0003g0003a0002c0002t0003g0004others(22): Show | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.433-964G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112407458 | |||||||
| chr10:112407488 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.433-934C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112407488 | |||||||
| chr10:112407545 | C | T | 67 | a0001c0001t0001g0165a0001c0001t0002g0001a0001c0001t0002g0045others(64): Show | 68 | HG00099.hp2 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.433-877C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112407545 | |||||||
| chr10:112407967 | C | T | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0181others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-455C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112407967 | |||||||
| chr10:112407983 | A | G | 181 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.433-439A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112407983 | |||||||
| chr10:112408229 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.433-193G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112408229 | |||||||
| chr10:112408276 | G | T | 1 | a0003c0004t0002g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.433-146G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | chr10 | 112408276 | |||||||
| chr10:112408298 | C | CA | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0027others(79): Show | 87 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.433-108dupA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr10 | 112408298 | ||||||
| chr10:112408611 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.532+90T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/20 | chr10 | 112408611 | |||||||
| chr10:112408911 | C | A | 34 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0260others(31): Show | 36 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.532+390C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/20 | chr10 | 112408911 | |||||||
| chr10:112408975 | T | C | 5 | a0001c0001t0002g0045a0001c0001t0002g0049a0001c0001t0002g0055others(2): Show | 5 | NA18994.hp2 NA18997.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+454T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/20 | chr10 | 112408975 | |||||||
| chr10:112408982 | G | A | 1 | a0001c0001t0002g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.532+461G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/20 | chr10 | 112408982 | |||||||
| chr10:112409097 | C | A | 1 | a0001c0001t0002g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.533-410C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/20 | chr10 | 112409097 | |||||||
| chr10:112409130 | T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-377T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/20 | chr10 | 112409130 | |||||||
| chr10:112409387 | G | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.533-120G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/20 | chr10 | 112409387 | |||||||
| chr10:112409432 | C | A | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(98): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.533-75C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 6/20 | chr10 | 112409432 | |||||||
| chr10:112409794 | G | A | 146 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(143): Show | 151 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.711+109G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 7/20 | chr10 | 112409794 | |||||||
| chr10:112409795 | T | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0178 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.711+110T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 7/20 | chr10 | 112409795 | |||||||
| chr10:112409906 | T | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(143): Show | 151 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.711+221T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 7/20 | chr10 | 112409906 | |||||||
| chr10:112409908 | A | G | 3 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0200 | 3 | HG02258.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.711+223A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 7/20 | chr10 | 112409908 | |||||||
| chr10:112409989 | G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0029 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.711+304G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 7/20 | chr10 | 112409989 | |||||||
| chr10:112410202 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.712-261T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 7/20 | chr10 | 112410202 | |||||||
| chr10:112410540 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.745-44C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 8/20 | chr10 | 112410540 | |||||||
| chr10:112410571 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.745-13C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 8/20 | chr10 | 112410571 | |||||||
| chr10:112410972 | T | C | 3 | a0001c0003t0002g0013a0001c0003t0002g0257a0001c0003t0002g0258 | 4 | HG02559.hp2 HG03225.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+337T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 9/20 | chr10 | 112410972 | |||||||
| chr10:112410992 | C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0046others(48): Show | 52 | HG00099.hp2 HG00597.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.796+357C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 9/20 | chr10 | 112410992 | |||||||
| chr10:112411426 | A | G | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0112others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.797-30A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 9/20 | chr10 | 112411426 | |||||||
| chr10:112411627 | T | TAC | 103 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(100): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.870+117_870+118dup others(2): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr10 | 112411627 | ||||||
| chr10:112411641 | C | T | 14 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.870+112C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 10/20 | chr10 | 112411641 | |||||||
| chr10:112411679 | G | A | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.870+150G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 10/20 | chr10 | 112411679 | |||||||
| chr10:112411841 | T | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0167others(39): Show | 45 | HG00738.hp2 HG01070.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.871-61T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 10/20 | chr10 | 112411841 | |||||||
| chr10:112412142 | C | T | 5 | a0001c0001t0002g0338a0001c0001t0002g0339a0001c0001t0002g0340others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.948+163C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | chr10 | 112412142 | |||||||
| chr10:112412318 | G | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0281 | 2 | NA19000.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.948+339G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | chr10 | 112412318 | |||||||
| chr10:112412423 | G | A | 10 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0112others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.948+444G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | chr10 | 112412423 | |||||||
| chr10:112412591 | TTC | T | 4 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324others(1): Show | 4 | HG01099.hp2 HG01192.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-574_949-573del others(2): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr10 | 112412591 | ||||||
| chr10:112412835 | C | T | 1 | a0001c0001t0006g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.949-338C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | chr10 | 112412835 | |||||||
| chr10:112412888 | T | TG | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.949-280dupG | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr10 | 112412888 | ||||||
| chr10:112412906 | C | T | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.949-267C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | chr10 | 112412906 | |||||||
| chr10:112413010 | G | A | 43 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0046others(40): Show | 44 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.949-163G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | chr10 | 112413010 | |||||||
| chr10:112413047 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.949-126C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 11/20 | chr10 | 112413047 | |||||||
| chr10:112413591 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1083+284G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112413591 | |||||||
| chr10:112413774 | T | A | 1 | a0001c0001t0002g0089 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1083+467T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112413774 | |||||||
| chr10:112413796 | G | A | 25 | a0002c0002t0001g0122a0002c0002t0003g0003a0002c0002t0003g0004others(22): Show | 27 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1083+489G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112413796 | |||||||
| chr10:112413894 | A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1083+587A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112413894 | |||||||
| chr10:112414352 | C | CT | 17 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0115others(14): Show | 17 | HG00597.hp2 HG01069.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1083+1066dupT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr10 | 112414352 | ||||||
| chr10:112414352 | CT | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 196 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1083+1066delT | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr10 | 112414352 | ||||||
| chr10:112414352 | CTT | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 7 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1083+1065_1083+106 others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr10 | 112414352 | ||||||
| chr10:112414354 | T | C | 4 | a0001c0001t0001g0224a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+1047T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112414354 | |||||||
| chr10:112414420 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1083+1113A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112414420 | |||||||
| chr10:112414500 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1083+1193G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112414500 | |||||||
| chr10:112414653 | C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0265 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1083+1346C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112414653 | |||||||
| chr10:112414673 | A | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1083+1366A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112414673 | |||||||
| chr10:112414711 | C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+1404C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112414711 | |||||||
| chr10:112415055 | C | G | 34 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0260others(31): Show | 36 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.1083+1748C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415055 | |||||||
| chr10:112415064 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1083+1757G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415064 | |||||||
| chr10:112415085 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1083+1778T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415085 | |||||||
| chr10:112415100 | T | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1084-1788T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415100 | |||||||
| chr10:112415171 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1084-1717C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415171 | |||||||
| chr10:112415196 | T | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1084-1692T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415196 | |||||||
| chr10:112415231 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1084-1657G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415231 | |||||||
| chr10:112415294 | G | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0004g0032others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-1594G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415294 | |||||||
| chr10:112415401 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1084-1487G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415401 | |||||||
| chr10:112415621 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1084-1267A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415621 | |||||||
| chr10:112415667 | C | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0103 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1084-1221C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415667 | |||||||
| chr10:112415890 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1084-998C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415890 | |||||||
| chr10:112415950 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1084-938G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112415950 | |||||||
| chr10:112416199 | T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0193 | 2 | HG02300.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1084-689T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416199 | |||||||
| chr10:112416210 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1084-678G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416210 | |||||||
| chr10:112416253 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1084-635C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416253 | |||||||
| chr10:112416267 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1084-621T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416267 | |||||||
| chr10:112416275 | T | C | 8 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0072others(5): Show | 8 | HG00597.hp2 NA18940.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-613T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416275 | |||||||
| chr10:112416287 | T | C | 1 | a0004c0006t0001g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1084-601T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416287 | |||||||
| chr10:112416383 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1084-505A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416383 | |||||||
| chr10:112416420 | G | A | 1 | a0002c0002t0001g0122 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1084-468G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416420 | |||||||
| chr10:112416462 | C | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0004g0032others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-426C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416462 | |||||||
| chr10:112416470 | C | CA | 140 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0042others(137): Show | 145 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.1084-393dupA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr10 | 112416470 | ||||||
| chr10:112416470 | C | CAA | 36 | a0001c0001t0001g0043a0001c0001t0001g0165a0001c0001t0002g0020others(33): Show | 37 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1084-394_1084-393d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr10 | 112416470 | ||||||
| chr10:112416470 | CA | C | 25 | a0001c0001t0001g0154a0001c0001t0001g0210a0001c0001t0001g0276others(22): Show | 27 | HG00323.hp2 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1084-393delA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr10 | 112416470 | ||||||
| chr10:112416488 | A | AG | 4 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-400_1084-399i others(3): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 12/20 | chr10 | 112416488 | |||||||
| chr10:112417201 | T | TAAAAA | 111 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0027others(108): Show | 117 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1218+191_1218+195d others(7): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr10 | 112417201 | ||||||
| chr10:112417201 | T | TAAAAAA | 91 | a0001c0001t0001g0006a0001c0001t0001g0112a0001c0001t0001g0165others(88): Show | 94 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.1218+190_1218+195d others(8): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr10 | 112417201 | ||||||
| chr10:112417201 | T | TAAAAAAA | 19 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0195others(16): Show | 19 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1218+189_1218+195d others(9): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr10 | 112417201 | ||||||
| chr10:112417201 | T | TAAAAAAA others(1): Show |
102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(99): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1218+188_1218+195d others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr10 | 112417201 | ||||||
| chr10:112417201 | T | TAAAAAAA others(2): Show |
7 | a0001c0001t0001g0172a0001c0001t0001g0188a0001c0001t0001g0251others(4): Show | 7 | HG00741.hp1 HG01517.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+187_1218+195d others(11): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr10 | 112417201 | ||||||
| chr10:112417222 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1218+200G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | chr10 | 112417222 | |||||||
| chr10:112417360 | G | A | 1 | a0002c0002t0003g0125 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1218+338G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | chr10 | 112417360 | |||||||
| chr10:112417410 | G | C | 1 | a0002c0002t0003g0121 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1218+388G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | chr10 | 112417410 | |||||||
| chr10:112417425 | C | G | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0112others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+403C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | chr10 | 112417425 | |||||||
| chr10:112417442 | G | T | 1 | a0001c0001t0006g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1219-404G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | chr10 | 112417442 | |||||||
| chr10:112417502 | CA | C | 20 | a0001c0001t0001g0018a0001c0001t0001g0170a0001c0001t0001g0224others(17): Show | 21 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1219-328delA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr10 | 112417502 | ||||||
| chr10:112417834 | T | A | 1 | a0001c0001t0003g0331 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1219-12T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 13/20 | chr10 | 112417834 | |||||||
| chr10:112418443 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1314+502G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112418443 | |||||||
| chr10:112418475 | G | A | 2 | a0004c0006t0001g0166a0004c0006t0001g0186 | 2 | HG01433.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1314+534G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112418475 | |||||||
| chr10:112418507 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1314+566G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112418507 | |||||||
| chr10:112418509 | C | G | 325 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(322): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1314+568C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112418509 | |||||||
| chr10:112418538 | C | T | 1 | a0002c0002t0001g0122 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1314+597C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112418538 | |||||||
| chr10:112418601 | A | T | 1 | a0001c0001t0002g0076 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1314+660A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112418601 | |||||||
| chr10:112418723 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1314+782A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112418723 | |||||||
| chr10:112418744 | T | A | 5 | a0001c0001t0002g0001a0001c0001t0002g0062a0001c0001t0002g0089others(2): Show | 6 | HG00609.hp2 HG01934.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+803T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112418744 | |||||||
| chr10:112419102 | C | CTG | 4 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG01081.hp2 HG01109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+1189_1314+119 others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr10 | 112419102 | ||||||
| chr10:112419102 | C | CTGTG | 18 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 19 | HG00558.hp1 HG01123.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1314+1187_1314+119 others(8): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr10 | 112419102 | ||||||
| chr10:112419102 | C | CTGTGTG | 21 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0133others(18): Show | 21 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1314+1185_1314+119 others(10): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr10 | 112419102 | ||||||
| chr10:112419102 | C | CTGTGTGT others(1): Show |
63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 67 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1314+1183_1314+119 others(12): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr10 | 112419102 | ||||||
| chr10:112419102 | C | CTGTGTGT others(3): Show |
9 | a0001c0001t0001g0213a0001c0001t0001g0221a0001c0001t0001g0237others(6): Show | 9 | HG00741.hp1 HG02155.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1314+1181_1314+119 others(14): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr10 | 112419102 | ||||||
| chr10:112419102 | C | CTGTGTGT others(5): Show |
4 | a0001c0001t0001g0014a0001c0001t0001g0232a0001c0001t0001g0236others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1314+1179_1314+119 others(16): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr10 | 112419102 | ||||||
| chr10:112419102 | CTG | C | 164 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0154others(161): Show | 170 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.1314+1189_1314+119 others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr10 | 112419102 | ||||||
| chr10:112419119 | T | C | 1 | a0001c0001t0002g0062 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1314+1178T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419119 | |||||||
| chr10:112419128 | GTGTA | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(17): Show | 21 | HG00738.hp2 HG01070.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1314+1188_1314+119 others(8): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419128 | |||||||
| chr10:112419130 | GTA | G | 27 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0041others(24): Show | 29 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1314+1190_1314+119 others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419130 | |||||||
| chr10:112419165 | G | C | 1 | a0001c0001t0002g0075 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1314+1224G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419165 | |||||||
| chr10:112419469 | G | T | 23 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0260others(20): Show | 25 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1314+1528G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419469 | |||||||
| chr10:112419525 | A | G | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.1314+1584A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419525 | |||||||
| chr10:112419598 | C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(96): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.1314+1657C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419598 | |||||||
| chr10:112419772 | C | G | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0112others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1315-1821C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419772 | |||||||
| chr10:112419911 | C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0264 | 2 | NA18954.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1315-1682C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112419911 | |||||||
| chr10:112420107 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1315-1486A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420107 | |||||||
| chr10:112420367 | G | T | 3 | a0001c0001t0002g0302a0001c0001t0002g0321a0006c0007t0002g0303 | 3 | HG02109.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1315-1226G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420367 | |||||||
| chr10:112420498 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1315-1095A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420498 | |||||||
| chr10:112420537 | C | A | 1 | a0001c0001t0002g0053 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1315-1056C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420537 | |||||||
| chr10:112420573 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1315-1020A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420573 | |||||||
| chr10:112420586 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1315-1007C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420586 | |||||||
| chr10:112420711 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1315-882C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420711 | |||||||
| chr10:112420820 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1315-773C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420820 | |||||||
| chr10:112420944 | A | G | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1315-649A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420944 | |||||||
| chr10:112420971 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1315-622C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112420971 | |||||||
| chr10:112421112 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1315-481A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112421112 | |||||||
| chr10:112421153 | C | T | 13 | a0001c0001t0002g0302a0001c0001t0002g0321a0001c0001t0002g0338others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1315-440C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112421153 | |||||||
| chr10:112421154 | G | A | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1315-439G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112421154 | |||||||
| chr10:112421189 | C | T | 1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1315-404C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112421189 | |||||||
| chr10:112421336 | G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1315-257G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112421336 | |||||||
| chr10:112421450 | C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0167others(35): Show | 41 | HG00738.hp2 HG01070.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1315-143C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 14/20 | chr10 | 112421450 | |||||||
| chr10:112421677 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1387+12A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 15/20 | chr10 | 112421677 | |||||||
| chr10:112421740 | T | G | 1 | a0001c0001t0001g0213 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1387+75T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 15/20 | chr10 | 112421740 | |||||||
| chr10:112421925 | A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(325): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1388-22A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 15/20 | chr10 | 112421925 | |||||||
| chr10:112422056 | G | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0112others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1476+21G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 16/20 | chr10 | 112422056 | |||||||
| chr10:112422101 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1476+66A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 16/20 | chr10 | 112422101 | |||||||
| chr10:112422179 | C | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0145 | 4 | HG02809.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+144C>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 16/20 | chr10 | 112422179 | |||||||
| chr10:112422241 | A | G | 1 | a0001c0001t0006g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1477-84A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 16/20 | chr10 | 112422241 | |||||||
| chr10:112422851 | C | CA | 5 | a0001c0001t0001g0009a0001c0001t0002g0081a0001c0001t0002g0085others(2): Show | 6 | HG02135.hp2 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1593+426dupA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112422851 | ||||||
| chr10:112422851 | CA | C | 9 | a0001c0001t0001g0234a0001c0001t0001g0255a0001c0001t0002g0049others(6): Show | 9 | HG01099.hp2 HG01928.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1593+426delA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112422851 | ||||||
| chr10:112422911 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1593+470G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112422911 | |||||||
| chr10:112423187 | CA | C | 22 | a0001c0001t0001g0008a0001c0001t0001g0217a0001c0001t0002g0020others(19): Show | 23 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1593+781delA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423187 | ||||||
| chr10:112423187 | CAAA | C | 32 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0219others(29): Show | 34 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1593+779_1593+781d others(5): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423187 | ||||||
| chr10:112423187 | CAAAA | C | 21 | a0001c0001t0001g0042a0001c0001t0001g0132a0001c0001t0001g0220others(18): Show | 21 | HG00323.hp2 HG01070.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1593+778_1593+781d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423187 | ||||||
| chr10:112423187 | CAAAAA | C | 11 | a0001c0001t0002g0024a0001c0001t0003g0331a0002c0002t0003g0003others(8): Show | 13 | HG02293.hp2 HG02818.hp1 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.1593+777_1593+781d others(7): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423187 | ||||||
| chr10:112423187 | CAAAAAA | C | 20 | a0001c0001t0003g0306a0001c0001t0003g0308a0001c0001t0003g0313others(17): Show | 20 | HG00544.hp2 HG01074.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1593+776_1593+781d others(8): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423187 | ||||||
| chr10:112423205 | A | AATATATA others(3): Show |
1 | a0001c0001t0004g0200 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1593+765_1593+766i others(12): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423205 | ||||||
| chr10:112423205 | A | AATATATA others(11): Show |
1 | a0001c0001t0004g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1593+765_1593+766i others(20): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423205 | ||||||
| chr10:112423205 | A | AATATATA others(17): Show |
1 | a0001c0001t0004g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1593+765_1593+766i others(26): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423205 | ||||||
| chr10:112423205 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0003g0019 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1593+766_1593+783d others(20): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423205 | ||||||
| chr10:112423207 | A | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0004g0032others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1593+766A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423207 | |||||||
| chr10:112423208 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1593+769_1593+791d others(25): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423208 | ||||||
| chr10:112423209 | A | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0004g0032others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1593+768A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423209 | |||||||
| chr10:112423211 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1593+770_1593+771i others(13): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423211 | |||||||
| chr10:112423211 | A | T | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0114others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1593+770A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423211 | |||||||
| chr10:112423212 | AAAAAAAA others(12): Show |
A | 3 | a0001c0003t0002g0013a0001c0003t0002g0257a0001c0003t0002g0258 | 3 | HG03225.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1593+773_1593+791d others(21): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423212 | ||||||
| chr10:112423213 | A | ATATATAT others(18): Show |
1 | a0001c0012t0001g0272 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1593+772_1593+773i others(27): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423213 | |||||||
| chr10:112423213 | A | T | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0113others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.1593+772A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423213 | |||||||
| chr10:112423213 | AAAAAAAA others(11): Show |
A | 1 | a0001c0003t0002g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1593+774_1593+791d others(20): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423213 | ||||||
| chr10:112423215 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1593+775_1593+776i others(12): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423215 | ||||||
| chr10:112423215 | A | AATATATA others(17): Show |
1 | a0001c0001t0001g0002 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1593+775_1593+776i others(26): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423215 | ||||||
| chr10:112423215 | A | ATATATAT others(8): Show |
1 | a0001c0001t0007g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1593+774_1593+775i others(17): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423215 | |||||||
| chr10:112423215 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0250 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1593+774_1593+775i others(33): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423215 | |||||||
| chr10:112423215 | A | T | 23 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0113others(20): Show | 23 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1593+774A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423215 | |||||||
| chr10:112423217 | A | AAT | 8 | a0001c0001t0002g0001a0001c0001t0002g0054a0001c0001t0002g0059others(5): Show | 8 | HG01934.hp2 HG02027.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1593+777_1593+778i others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423217 | ||||||
| chr10:112423217 | A | AATATATA others(19): Show |
1 | a0001c0001t0001g0211 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1593+777_1593+778i others(28): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423217 | ||||||
| chr10:112423217 | A | AATATATA others(23): Show |
2 | a0001c0001t0001g0227a0001c0001t0001g0283 | 2 | HG00099.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1593+777_1593+778i others(32): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423217 | ||||||
| chr10:112423217 | A | AATATATA others(27): Show |
1 | a0001c0001t0001g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1593+777_1593+778i others(36): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423217 | ||||||
| chr10:112423217 | A | AATATATA others(29): Show |
3 | a0001c0001t0001g0191a0001c0001t0001g0251a0001c0001t0001g0275 | 3 | HG02683.hp2 NA19078.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1593+777_1593+778i others(38): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423217 | ||||||
| chr10:112423217 | A | AT | 11 | a0001c0001t0002g0047a0001c0001t0002g0050a0001c0001t0002g0051others(8): Show | 11 | HG00642.hp2 HG01358.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1593+776_1593+777i others(3): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423217 | |||||||
| chr10:112423217 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0266 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1593+776_1593+777i others(33): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423217 | |||||||
| chr10:112423217 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1593+776_1593+777i others(41): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423217 | |||||||
| chr10:112423217 | A | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0034others(85): Show | 92 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1593+776A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423217 | |||||||
| chr10:112423219 | A | AATATATA others(7): Show |
1 | a0001c0001t0002g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1593+779_1593+780i others(16): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(9): Show |
2 | a0001c0001t0001g0168a0001c0001t0001g0210 | 2 | HG00558.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1593+779_1593+780i others(18): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(19): Show |
1 | a0007c0011t0001g0179 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1593+779_1593+780i others(28): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0255 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1593+779_1593+780i others(30): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(23): Show |
1 | a0001c0001t0001g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1593+779_1593+780i others(32): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(25): Show |
1 | a0001c0001t0001g0005 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1593+779_1593+780i others(34): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(27): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0264 | 2 | NA18954.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1593+779_1593+780i others(36): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(29): Show |
1 | a0001c0001t0001g0027 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1593+779_1593+780i others(38): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(31): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0174a0001c0001t0001g0290 | 3 | HG00733.hp1 HG02735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1593+779_1593+780i others(40): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(33): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0288 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1593+779_1593+780i others(42): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(35): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0209 | 3 | HG00323.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1593+779_1593+780i others(44): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AATATATA others(43): Show |
1 | a0001c0001t0001g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1593+779_1593+780i others(52): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423219 | A | AT | 3 | a0001c0001t0002g0046a0001c0001t0002g0067a0001c0001t0002g0323 | 3 | HG01978.hp2 HG02735.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1593+778_1593+779i others(3): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0233 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1593+778_1593+779i others(15): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0010a0001c0001t0001g0207a0001c0001t0001g0228 | 3 | NA18612.hp1 NA19001.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1593+778_1593+779i others(23): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1593+778_1593+779i others(27): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | ATATATAT others(20): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0235a0001c0001t0001g0270 | 3 | NA19058.hp1 NA19062.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1593+778_1593+779i others(29): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1593+778_1593+779i others(31): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | ATATATAT others(24): Show |
2 | a0001c0001t0001g0226a0001c0001t0001g0249 | 2 | HG00639.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1593+778_1593+779i others(33): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1593+778_1593+779i others(39): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | ATATATAT others(113): Show |
1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1593+778_1593+779i others(122): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | A | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0034others(160): Show | 170 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1593+778A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423219 | |||||||
| chr10:112423219 | AAAATATA others(3): Show |
A | 1 | a0001c0001t0001g0237 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1593+780_1593+789d others(12): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423219 | ||||||
| chr10:112423221 | A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(44): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(46): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAAAAA others(36): Show |
1 | a0001c0001t0001g0196 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(45): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAAAAA others(41): Show |
1 | a0001c0001t0001g0193 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(50): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAAATA others(25): Show |
1 | a0001c0001t0001g0271 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(34): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAAATA others(35): Show |
1 | a0001c0001t0001g0170 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(44): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAATAT others(22): Show |
1 | a0001c0001t0001g0215 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(31): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAATAT others(28): Show |
1 | a0001c0001t0001g0273 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(37): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAATAT others(30): Show |
1 | a0001c0001t0001g0190 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(39): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAATAT others(32): Show |
1 | a0001c0001t0001g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(41): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAAATAT others(34): Show |
2 | a0001c0001t0001g0182a0001c0001t0002g0204 | 2 | HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1593+781_1593+782i others(43): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0243 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(22): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAATATA others(17): Show |
1 | a0001c0001t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(26): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAATATA others(21): Show |
1 | a0001c0001t0001g0152 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(30): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAATATA others(25): Show |
1 | a0001c0001t0001g0241 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(34): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAATATA others(27): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0178 | 2 | HG02080.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1593+781_1593+782i others(36): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAATATA others(33): Show |
1 | a0001c0001t0001g0203 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(42): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAATATA others(35): Show |
1 | a0001c0001t0001g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(44): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAAATATA others(51): Show |
1 | a0001c0001t0001g0265 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(60): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(12): Show |
1 | a0001c0001t0001g0274 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(21): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(16): Show |
1 | a0001c0001t0001g0205 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(25): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(18): Show |
1 | a0001c0001t0001g0240 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(27): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(20): Show |
1 | a0001c0001t0001g0284 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(29): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(22): Show |
1 | a0001c0001t0001g0256 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(31): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(28): Show |
2 | a0001c0001t0001g0173a0001c0001t0001g0289 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1593+781_1593+782i others(37): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(30): Show |
3 | a0001c0001t0001g0153a0001c0001t0001g0248a0001c0005t0001g0252 | 3 | HG01361.hp1 HG01361.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1593+781_1593+782i others(39): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(32): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0224a0001c0001t0001g0347 | 3 | HG01175.hp1 HG01943.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1593+781_1593+782i others(41): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(40): Show |
1 | a0001c0001t0001g0189 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1593+781_1593+782i others(49): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(42): Show |
1 | a0001c0001t0001g0229 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(51): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AAATATAT others(46): Show |
1 | a0001c0001t0001g0259 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1593+781_1593+782i others(55): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(19): Show |
3 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0002g0007 | 3 | HG02647.hp1 HG03098.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1593+803_1593+804i others(28): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(23): Show |
3 | a0001c0001t0001g0212a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | NA18940.hp2 NA18972.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1593+803_1593+804i others(32): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(25): Show |
1 | a0001c0001t0001g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1593+803_1593+804i others(34): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(27): Show |
3 | a0001c0001t0001g0127a0001c0001t0001g0201a0001c0001t0001g0213 | 3 | HG02572.hp2 NA18964.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1593+803_1593+804i others(36): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(29): Show |
2 | a0001c0001t0001g0263a0001c0001t0001g0277 | 2 | HG01928.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1593+803_1593+804i others(38): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(33): Show |
1 | a0001c0001t0001g0239 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1593+803_1593+804i others(42): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(35): Show |
1 | a0001c0001t0001g0188 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1593+803_1593+804i others(44): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(37): Show |
4 | a0001c0001t0001g0137a0001c0001t0001g0231a0001c0001t0001g0280others(1): Show | 4 | HG01255.hp2 HG02004.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1593+803_1593+804i others(46): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(39): Show |
1 | a0001c0001t0001g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1593+803_1593+804i others(48): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | AATATATA others(41): Show |
1 | a0001c0001t0001g0177 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1593+803_1593+804i others(50): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423221 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0223 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1593+780_1593+781i others(19): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0214 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1593+780_1593+781i others(21): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0232 | 2 | HG02683.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1593+780_1593+781i others(25): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0278 | 2 | HG00609.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1593+780_1593+781i others(29): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(22): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0242a0001c0001t0001g0295others(1): Show | 4 | HG00140.hp1 HG01517.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1593+780_1593+781i others(31): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(24): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0247a0001c0001t0002g0199 | 3 | HG02976.hp2 NA18966.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1593+780_1593+781i others(33): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(26): Show |
9 | a0001c0001t0001g0012a0001c0001t0001g0176a0001c0001t0001g0181others(6): Show | 9 | HG00140.hp2 HG02630.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1593+780_1593+781i others(35): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(28): Show |
4 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0202others(1): Show | 5 | HG02129.hp1 HG03490.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1593+780_1593+781i others(37): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0345 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1593+780_1593+781i others(39): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | ATATATAT others(36): Show |
3 | a0001c0001t0001g0133a0001c0001t0001g0187a0001c0001t0001g0234 | 3 | HG01515.hp2 NA18984.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1593+780_1593+781i others(45): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | A | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.1593+780A>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423221 | |||||||
| chr10:112423221 | AATATATA others(3): Show |
A | 2 | a0001c0001t0001g0180a0001c0001t0001g0183 | 2 | NA18999.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1593+794_1593+803d others(12): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr10 | 112423221 | ||||||
| chr10:112423222 | ATAT | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0146a0001c0001t0001g0150others(1): Show | 4 | HG01175.hp2 HG03688.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1593+782_1593+784d others(5): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423222 | |||||||
| chr10:112423225 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1593+784T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423225 | |||||||
| chr10:112423325 | C | T | 2 | a0001c0003t0002g0013a0001c0003t0002g0258 | 3 | HG02559.hp2 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1593+884C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423325 | |||||||
| chr10:112423487 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1593+1046A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423487 | |||||||
| chr10:112423793 | G | T | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1593+1352G>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423793 | |||||||
| chr10:112423846 | C | T | 3 | a0001c0001t0002g0067a0001c0001t0002g0088a0001c0001t0002g0326 | 3 | HG01074.hp2 HG01358.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1593+1405C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112423846 | |||||||
| chr10:112424401 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1594-937G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112424401 | |||||||
| chr10:112424580 | T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0167a0001c0001t0001g0173others(14): Show | 19 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1594-758T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112424580 | |||||||
| chr10:112424634 | C | T | 2 | a0001c0001t0002g0324a0001c0001t0002g0336 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1594-704C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112424634 | |||||||
| chr10:112424635 | G | A | 1 | a0001c0001t0003g0317 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1594-703G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112424635 | |||||||
| chr10:112424734 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1594-604T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112424734 | |||||||
| chr10:112425113 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1594-225G>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112425113 | |||||||
| chr10:112425167 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1594-171C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 17/20 | chr10 | 112425167 | |||||||
| chr10:112425595 | T | TA | 19 | a0001c0001t0001g0165a0001c0001t0002g0050a0001c0001t0002g0051others(16): Show | 19 | HG00642.hp2 HG01074.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1737+131dupA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr10 | 112425595 | ||||||
| chr10:112425595 | T | TAA | 49 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0046others(46): Show | 50 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1737+130_1737+131d others(4): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr10 | 112425595 | ||||||
| chr10:112425595 | TA | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 81 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1737+131delA | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr10 | 112425595 | ||||||
| chr10:112425807 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1737+326A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 18/20 | chr10 | 112425807 | |||||||
| chr10:112425854 | CAAAA | C | 4 | a0001c0001t0002g0070a0001c0001t0002g0097a0001c0001t0002g0098others(1): Show | 4 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+374_1737+377d others(6): Show |
ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 18/20 | chr10 | 112425854 | |||||||
| chr10:112425916 | C | T | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG02976.hp1 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-342C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 18/20 | chr10 | 112425916 | |||||||
| chr10:112426098 | T | TG | 329 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(326): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1738-158dupG | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr10 | 112426098 | ||||||
| chr10:112426399 | C | T | 41 | a0001c0001t0002g0338a0001c0001t0002g0339a0001c0001t0002g0340others(38): Show | 43 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1839+40C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 19/20 | chr10 | 112426399 | |||||||
| chr10:112426420 | C | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG02258.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1839+61C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 19/20 | chr10 | 112426420 | |||||||
| chr10:112426466 | A | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0275 | 3 | HG01515.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1839+107A>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 19/20 | chr10 | 112426466 | |||||||
| chr10:112426569 | A | C | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0312 | 3 | NA19005.hp2 NA19006.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1839+210A>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 19/20 | chr10 | 112426569 | |||||||
| chr10:112426860 | G | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | splice_donor_variant&intron_variant | HIGH | c.1911+1G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426860 | |||||||
| chr10:112426862 | G | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | splice_region_variant&intron_variant | LOW | c.1911+3G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426862 | |||||||
| chr10:112426864 | G | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | splice_region_variant&intron_variant | LOW | c.1911+5G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426864 | |||||||
| chr10:112426865 | T | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | splice_region_variant&intron_variant | LOW | c.1911+6T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426865 | |||||||
| chr10:112426866 | G | A | 334 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(331): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
splice_region_variant&intron_variant | LOW | c.1911+7G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426866 | |||||||
| chr10:112426867 | C | T | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | splice_region_variant&intron_variant | LOW | c.1911+8C>T | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426867 | |||||||
| chr10:112426868 | T | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911+9T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426868 | |||||||
| chr10:112426870 | C | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911+11C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426870 | |||||||
| chr10:112426871 | C | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911+12C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426871 | |||||||
| chr10:112426873 | C | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911+14C>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426873 | |||||||
| chr10:112426877 | T | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911+18T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426877 | |||||||
| chr10:112426878 | G | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911+19G>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426878 | |||||||
| chr10:112426879 | T | G | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911+20T>G | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426879 | |||||||
| chr10:112426880 | T | A | 1 | a0001c0001t0005g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911+21T>A | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112426880 | |||||||
| chr10:112427076 | T | C | 4 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0200others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1912-142T>C | ACSL5 | ENSG00000197142.11 | transcript | ENST00000354655.9 | protein_coding | 20/20 | chr10 | 112427076 |