Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2180 |
| ensemblid | ENSG00000151726.16 |
| hgncid | 3569 |
| symbol | ACSL1 |
| name | acyl-CoA synthetase long chain family member 1 |
| refseq_nuc | NM_001995.5 |
| refseq_prot | NP_001986.2 |
| ensembl_nuc | ENST00000281455.7 |
| ensembl_prot | ENSP00000281455.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 184755595 |
| end | 184825968 |
| strand | - |
| ver | v1.2 |
| region | chr4:184755595-184825968 |
| region5000 | chr4:184750595-184830968 |
| regionname0 | ACSL1_chr4_184755595_184825968 |
| regionname5000 | ACSL1_chr4_184750595_184830968 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 698 | 390 | 95 | 71 | 166 | 14 | 42 | 130 | ACSL1_chr4_184750595_184830968 | ACSL1 | MQAHE others(693): Show |
chr4 | 184750595 | 184830968 |
| a0002 | 0/0 | 698 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | MQAHE others(693): Show |
chr4 | 184750595 | 184830968 |
| a0003 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | MQAHE others(693): Show |
chr4 | 184750595 | 184830968 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2094 | 241 | 68 | 36 | 106 | 10 | 21 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0002 | 0/1 | 2094 | 73 | 18 | 10 | 34 | 2 | 8 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0003 | 0/0 | 2094 | 42 | 3 | 13 | 14 | 2 | 10 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0004 | 0/0 | 2094 | 12 | 0 | 7 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0005 | 1/0 | 2094 | 9 | 4 | 0 | 2 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0006 | 0/0 | 2094 | 5 | 0 | 0 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0007 | 0/0 | 2094 | 3 | 2 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0008 | 0/0 | 2094 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0009 | 0/0 | 2094 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0001c0010 | 0/0 | 2094 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0002c0011 | 0/0 | 2094 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 | ||
| a0003c0012 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | ATGCA others(2089): Show |
chr4 | 184750595 | 184830968 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3712 | 151 | 30 | 12 | 93 | 5 | 11 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0001t0002 | 0/0 | 3712 | 60 | 35 | 10 | 10 | 2 | 3 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0001t0003 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0001t0004 | 0/0 | 3712 | 23 | 2 | 12 | 0 | 2 | 7 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0001t0005 | 0/0 | 3712 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0001t0008 | 0/0 | 3712 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0001t0009 | 0/0 | 3712 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0001t0010 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0001t0011 | 0/0 | 3712 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0002t0002 | 0/1 | 3712 | 71 | 17 | 9 | 34 | 2 | 8 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0002t0004 | 0/0 | 3712 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0002t0007 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0003t0003 | 0/0 | 3712 | 41 | 3 | 13 | 14 | 2 | 9 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0003t0013 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0004t0001 | 0/0 | 3712 | 12 | 0 | 7 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0005t0001 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0005t0002 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0005t0003 | 0/0 | 3712 | 3 | 1 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0005t0006 | 1/0 | 3712 | 2 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0005t0012 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0005t0014 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0006t0002 | 0/0 | 3712 | 5 | 0 | 0 | 5 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0007t0002 | 0/0 | 3712 | 3 | 2 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0008t0004 | 0/0 | 3712 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0009t0002 | 0/0 | 3712 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0001c0010t0001 | 0/0 | 3712 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0002c0011t0001 | 0/0 | 3712 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| a0003c0012t0002 | 0/0 | 3712 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | AGGGA others(3707): Show |
chr4 | 184750595 | 184830968 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0009g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0002t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0003t0013g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0004t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0006g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0005t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0006t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0007t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0007t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0007t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0008t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0008t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0009t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0009t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0001c0010t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0002c0011t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| a0003c0012t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0200 | EUR | GBR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0076 | EUR | GBR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00280 | hp1 | a0001 | c0003 | t0003 | g0263 | EUR | FIN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | FIN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0097 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0268 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00639 | hp1 | a0001 | c0009 | t0002 | g0140 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00639 | hp2 | a0001 | c0008 | t0004 | g0297 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00642 | hp1 | a0001 | c0003 | t0003 | g0256 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0059 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00673 | hp1 | a0001 | c0001 | t0008 | g0063 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | CHS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00733 | hp1 | a0001 | c0008 | t0004 | g0304 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00738 | hp1 | a0002 | c0011 | t0001 | g0328 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00738 | hp2 | a0001 | c0009 | t0002 | g0090 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0309 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0357 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0321 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01070 | hp1 | a0001 | c0003 | t0003 | g0310 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0290 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0322 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01071 | hp2 | a0001 | c0003 | t0003 | g0312 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01081 | hp2 | a0001 | c0007 | t0002 | g0154 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0276 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0213 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0356 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01168 | hp2 | a0001 | c0003 | t0003 | g0308 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0355 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01256 | hp1 | a0001 | c0003 | t0003 | g0141 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0147 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01257 | hp1 | a0001 | c0003 | t0003 | g0018 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01258 | hp1 | a0001 | c0003 | t0003 | g0142 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0018 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0267 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0354 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0197 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0311 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0338 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0236 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0296 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0343 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | IBS | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01891 | hp1 | a0001 | c0005 | t0003 | g0219 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0346 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0332 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01928 | hp2 | a0001 | c0004 | t0001 | g0104 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0330 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0284 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0246 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02015 | hp2 | a0001 | c0005 | t0003 | g0262 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0270 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02040 | hp2 | a0001 | c0005 | t0003 | g0050 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02055 | hp1 | a0001 | c0003 | t0003 | g0180 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02083 | hp1 | a0001 | c0004 | t0001 | g0269 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0277 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | CDX | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | CDX | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CDX | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0228 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02258 | hp2 | a0003 | c0012 | t0002 | g0150 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | PEL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02451 | hp1 | a0001 | c0007 | t0002 | g0152 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0353 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02602 | hp1 | a0001 | c0005 | t0002 | g0288 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0110 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0364 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02683 | hp2 | a0001 | c0003 | t0003 | g0012 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02723 | hp2 | a0001 | c0005 | t0006 | g0227 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0326 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0138 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0038 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0365 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0352 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03017 | hp2 | a0001 | c0010 | t0001 | g0302 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0366 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0363 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03209 | hp1 | a0001 | c0005 | t0014 | g0151 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0339 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0264 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0301 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03516 | hp1 | a0001 | c0002 | t0007 | g0347 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0218 | AFR | ESN | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0156 | AFR | GWD | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03669 | hp1 | a0001 | c0003 | t0003 | g0241 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0096 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0335 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0012 | SAS | PJL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03831 | hp1 | a0001 | c0003 | t0013 | g0265 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03831 | hp2 | a0001 | c0003 | t0003 | g0278 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03834 | hp1 | a0001 | c0003 | t0003 | g0266 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0056 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03942 | hp2 | a0001 | c0003 | t0003 | g0329 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0305 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0128 | SAS | BEB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0289 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0295 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04228 | hp1 | a0001 | c0005 | t0001 | g0334 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0146 | SAS | STU | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | CHB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0340 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18947 | hp1 | a0001 | c0003 | t0003 | g0081 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18950 | hp2 | a0001 | c0003 | t0003 | g0232 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18965 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18966 | hp2 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18973 | hp2 | a0001 | c0006 | t0002 | g0037 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18979 | hp1 | a0001 | c0006 | t0002 | g0201 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0062 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18984 | hp1 | a0001 | c0001 | t0009 | g0341 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19000 | hp1 | a0001 | c0003 | t0003 | g0026 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19002 | hp2 | a0001 | c0003 | t0003 | g0233 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19005 | hp1 | a0001 | c0006 | t0002 | g0087 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0047 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19010 | hp1 | a0001 | c0003 | t0003 | g0094 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19030 | hp2 | a0001 | c0007 | t0002 | g0153 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0029 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19056 | hp1 | a0001 | c0006 | t0002 | g0249 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19063 | hp2 | a0001 | c0001 | t0011 | g0066 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19068 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19075 | hp1 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19076 | hp2 | a0001 | c0006 | t0002 | g0291 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | YRI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ASW | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ASW | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0320 | EUR | TSI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0143 | EUR | TSI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20805 | hp1 | a0001 | c0003 | t0003 | g0045 | EUR | TSI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0337 | EUR | TSI | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0314 | SAS | GIH | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0351 | SAS | GIH | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | CLM | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0068 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0303 | AFR | ACB | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03471 | hp1 | a0001 | c0005 | t0012 | g0149 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0362 | AFR | MSL | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | USA | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0105 | AFR | USA | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA20300 | hp2 | a0001 | c0003 | t0003 | g0349 | AFR | USA | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0157 | AFR | LWK | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0239 | REF | REF | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0006 | g0211 | REF | REF | ACSL1_chr4_184750595_184830968 | ACSL1 | chr4 | 184750595 | 184830968 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184773859 | T | A | 1 | a0002 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.773A>T | p.Asn258Ile | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 8/21 | 858/3712 | 773/2097 | 258/698 | chr4 | 184773859 | |||
| chr4:184776913 | T | C | 1 | a0003 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.548A>G | p.Asn183Ser | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 6/21 | 633/3712 | 548/2097 | 183/698 | chr4 | 184776913 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184757686 | G | A | 1 | a0001c0006 | 5 | NA18973.hp2 NA18979.hp1 NA19005.hp1 others(2): Show |
synonymous_variant | LOW | c.1905C>T | p.Leu635Leu | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 20/21 | 1990/3712 | 1905/2097 | 635/698 | chr4 | 184757686 | |||
| chr4:184760360 | C | A | 1 | a0001c0008 | 2 | HG00639.hp2 HG00733.hp1 |
synonymous_variant | LOW | c.1779G>T | p.Leu593Leu | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/21 | 1864/3712 | 1779/2097 | 593/698 | chr4 | 184760360 | |||
| chr4:184762473 | C | T | 1 | a0001c0007 | 3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1572G>A | p.Ala524Ala | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/21 | 1657/3712 | 1572/2097 | 524/698 | chr4 | 184762473 | |||
| chr4:184764878 | C | T | 10 | a0001c0001 a0001c0002 a0001c0004 others(7): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(337): Show |
synonymous_variant | LOW | c.1407G>A | p.Leu469Leu | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/21 | 1492/3712 | 1407/2097 | 469/698 | chr4 | 184764878 | |||
| chr4:184764911 | G | A | 1 | a0001c0009 | 2 | HG00639.hp1 HG00738.hp2 |
synonymous_variant | LOW | c.1374C>T | p.Tyr458Tyr | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/21 | 1459/3712 | 1374/2097 | 458/698 | chr4 | 184764911 | |||
| chr4:184765975 | G | A | 2 | a0001c0004 a0002c0011 |
13 | HG00609.hp2 HG00738.hp1 HG01123.hp1 others(10): Show |
synonymous_variant | LOW | c.1275C>T | p.Gly425Gly | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/21 | 1360/3712 | 1275/2097 | 425/698 | chr4 | 184765975 | |||
| chr4:184766709 | A | G | 5 | a0001c0002 a0001c0006 a0001c0008 others(2): Show |
82 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(79): Show |
synonymous_variant | LOW | c.1176T>C | p.Phe392Phe | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/21 | 1261/3712 | 1176/2097 | 392/698 | chr4 | 184766709 | |||
| chr4:184766717 | A | G | 1 | a0001c0010 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1168T>C | p.Leu390Leu | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/21 | 1253/3712 | 1168/2097 | 390/698 | chr4 | 184766717 | |||
| chr4:184780395 | G | T | 1 | a0001c0003 | 42 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(39): Show |
synonymous_variant | LOW | c.414C>A | p.Ile138Ile | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/21 | 499/3712 | 414/2097 | 138/698 | chr4 | 184780395 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184755898 | G | T | 1 | a0001c0001t0010 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1227C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 1227 | chr4 | 184755898 | ||||||
| chr4:184755983 | A | G | 1 | a0001c0001t0009 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 1142 | chr4 | 184755983 | ||||||
| chr4:184756209 | T | C | 3 | a0001c0001t0004 a0001c0002t0004 a0001c0008t0004 |
26 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*916A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 916 | chr4 | 184756209 | ||||||
| chr4:184756267 | C | T | 4 | a0001c0001t0003 a0001c0003t0003 a0001c0003t0013 others(1): Show |
46 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*858G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 858 | chr4 | 184756267 | ||||||
| chr4:184756431 | C | T | 1 | a0001c0001t0008 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*694G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 694 | chr4 | 184756431 | ||||||
| chr4:184756434 | G | A | 1 | a0001c0003t0013 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*691C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 691 | chr4 | 184756434 | ||||||
| chr4:184756710 | T | G | 1 | a0001c0001t0005 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*415A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 415 | chr4 | 184756710 | ||||||
| chr4:184756798 | G | A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
3_prime_UTR_variant | MODIFIER | c.*327C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 327 | chr4 | 184756798 | ||||||
| chr4:184756927 | T | C | 1 | a0001c0001t0011 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 198 | chr4 | 184756927 | ||||||
| chr4:184756956 | A | G | 10 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(7): Show |
172 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 169 | chr4 | 184756956 | ||||||
| chr4:184756964 | C | G | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 161 | chr4 | 184756964 | ||||||
| chr4:184757007 | T | C | 1 | a0001c0005t0014 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*118A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 118 | chr4 | 184757007 | ||||||
| chr4:184757029 | C | T | 1 | a0001c0002t0007 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 21/21 | 96 | chr4 | 184757029 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184757336 | T | C | 4 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0023 others(1): Show |
5 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1957-71A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 20/20 | chr4 | 184757336 | |||||||
| chr4:184757402 | A | C | 1 | a0001c0001t0002g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1957-137T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 20/20 | chr4 | 184757402 | |||||||
| chr4:184757439 | G | T | 1 | a0001c0003t0003g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1957-174C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 20/20 | chr4 | 184757439 | |||||||
| chr4:184757937 | T | C | 11 | a0001c0001t0002g0014 a0001c0001t0002g0159 a0001c0001t0002g0160 others(8): Show |
12 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1783-17A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184757937 | |||||||
| chr4:184758022 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1783-102T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758022 | |||||||
| chr4:184758053 | A | AC | 11 | a0001c0001t0001g0043 a0001c0001t0001g0108 a0001c0001t0001g0122 others(8): Show |
11 | NA18747.hp1 NA18940.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.1783-134dupG | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758053 | |||||||
| chr4:184758185 | C | T | 144 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0001g0345 others(141): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1783-265G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758185 | |||||||
| chr4:184758263 | A | T | 1 | a0001c0001t0011g0066 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1783-343T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758263 | |||||||
| chr4:184758314 | G | T | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1783-394C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758314 | |||||||
| chr4:184758352 | C | T | 2 | a0001c0005t0012g0149 a0001c0005t0014g0151 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1783-432G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758352 | |||||||
| chr4:184758353 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1783-433C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758353 | |||||||
| chr4:184758469 | C | T | 52 | a0001c0001t0001g0020 a0001c0001t0001g0171 a0001c0001t0001g0210 others(49): Show |
58 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1783-549G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758469 | |||||||
| chr4:184758509 | C | CT | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1783-590dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758509 | |||||||
| chr4:184758522 | C | G | 14 | a0001c0001t0004g0048 a0001c0001t0004g0138 a0001c0001t0004g0139 others(11): Show |
14 | HG00735.hp1 HG01106.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1783-602G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758522 | |||||||
| chr4:184758661 | G | A | 25 | a0001c0001t0004g0048 a0001c0001t0004g0138 a0001c0001t0004g0139 others(22): Show |
25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1783-741C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758661 | |||||||
| chr4:184758684 | T | C | 4 | a0001c0002t0002g0036 a0001c0002t0002g0128 a0001c0009t0002g0090 others(1): Show |
4 | HG00639.hp1 HG00738.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783-764A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758684 | |||||||
| chr4:184758757 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1783-837T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758757 | |||||||
| chr4:184758775 | T | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
162 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.1783-855A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758775 | |||||||
| chr4:184758819 | G | T | 1 | a0001c0001t0002g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1783-899C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758819 | |||||||
| chr4:184758836 | G | C | 41 | a0001c0001t0003g0343 a0001c0003t0003g0006 a0001c0003t0003g0012 others(38): Show |
45 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1783-916C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184758836 | |||||||
| chr4:184759003 | G | GT | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1783-1084dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759003 | |||||||
| chr4:184759012 | C | G | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1783-1092G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759012 | |||||||
| chr4:184759036 | A | G | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0313 others(1): Show |
4 | HG01081.hp1 HG01243.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1783-1116T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759036 | |||||||
| chr4:184759193 | G | C | 4 | a0001c0002t0002g0005 a0001c0002t0002g0049 a0001c0002t0002g0068 others(1): Show |
5 | HG00741.hp1 HG02027.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1782+1164C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759193 | |||||||
| chr4:184759397 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1782+960C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759397 | |||||||
| chr4:184759409 | A | G | 25 | a0001c0001t0004g0048 a0001c0001t0004g0138 a0001c0001t0004g0139 others(22): Show |
25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1782+948T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759409 | |||||||
| chr4:184759412 | G | A | 49 | a0001c0001t0001g0345 a0001c0001t0002g0016 a0001c0001t0002g0022 others(46): Show |
54 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1782+945C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759412 | |||||||
| chr4:184759711 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(52): Show |
62 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1782+646A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184759711 | |||||||
| chr4:184760279 | A | G | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1782+78T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184760279 | |||||||
| chr4:184760296 | C | T | 7 | a0001c0001t0002g0088 a0001c0001t0002g0148 a0001c0001t0002g0158 others(4): Show |
7 | HG01975.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1782+61G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184760296 | |||||||
| chr4:184760321 | G | C | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1782+36C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 18/20 | chr4 | 184760321 | |||||||
| chr4:184760599 | T | C | 11 | a0001c0001t0004g0335 a0001c0001t0004g0337 a0001c0001t0004g0338 others(8): Show |
11 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1639-99A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184760599 | |||||||
| chr4:184760966 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0122 a0001c0001t0001g0281 |
3 | NA18940.hp2 NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1639-466C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184760966 | |||||||
| chr4:184761029 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1639-529T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761029 | |||||||
| chr4:184761099 | C | T | 7 | a0001c0001t0002g0088 a0001c0001t0002g0148 a0001c0001t0002g0158 others(4): Show |
7 | HG01975.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639-599G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761099 | |||||||
| chr4:184761119 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1639-619T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761119 | |||||||
| chr4:184761166 | C | T | 5 | a0001c0002t0002g0024 a0001c0002t0002g0053 a0001c0002t0002g0054 others(2): Show |
5 | HG00438.hp2 HG00558.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1639-666G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761166 | |||||||
| chr4:184761240 | A | T | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1639-740T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761240 | |||||||
| chr4:184761413 | A | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1639-913T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761413 | |||||||
| chr4:184761461 | A | C | 44 | a0001c0001t0003g0343 a0001c0003t0003g0006 a0001c0003t0003g0012 others(41): Show |
48 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1638+946T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761461 | |||||||
| chr4:184761480 | A | G | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1638+927T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761480 | |||||||
| chr4:184761540 | A | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
278 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.1638+867T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761540 | |||||||
| chr4:184761672 | C | A | 1 | a0001c0004t0001g0270 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1638+735G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761672 | |||||||
| chr4:184761783 | T | C | 3 | a0001c0002t0002g0008 a0001c0002t0002g0070 a0001c0002t0002g0273 |
4 | NA18612.hp2 NA18962.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638+624A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761783 | |||||||
| chr4:184761820 | A | T | 1 | a0001c0001t0002g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1638+587T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761820 | |||||||
| chr4:184761956 | G | A | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1638+451C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184761956 | |||||||
| chr4:184762083 | C | T | 3 | a0001c0001t0002g0158 a0001c0001t0002g0364 a0001c0001t0002g0365 |
3 | HG02486.hp1 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1638+324G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762083 | |||||||
| chr4:184762084 | G | A | 14 | a0001c0001t0004g0048 a0001c0001t0004g0138 a0001c0001t0004g0139 others(11): Show |
14 | HG00735.hp1 HG01106.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1638+323C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762084 | |||||||
| chr4:184762126 | C | T | 11 | a0001c0001t0002g0014 a0001c0001t0002g0159 a0001c0001t0002g0160 others(8): Show |
12 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638+281G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762126 | |||||||
| chr4:184762131 | C | CA | 25 | a0001c0001t0001g0079 a0001c0001t0001g0274 a0001c0001t0001g0318 others(22): Show |
25 | HG00639.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1638+275dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762131 | |||||||
| chr4:184762131 | C | CAA | 7 | a0001c0001t0001g0345 a0001c0001t0002g0016 a0001c0001t0002g0022 others(4): Show |
8 | HG00733.hp2 HG01358.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638+274_1638+275d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762131 | |||||||
| chr4:184762236 | ACCCTGTC | A | 5 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0023 others(2): Show |
6 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638+164_1638+170d others(9): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762236 | |||||||
| chr4:184762238 | C | A | 1 | a0001c0001t0002g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1638+169G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 17/20 | chr4 | 184762238 | |||||||
| chr4:184762596 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1522-73A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762596 | |||||||
| chr4:184762686 | A | G | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(360): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.1522-163T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762686 | |||||||
| chr4:184762790 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1522-267G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762790 | |||||||
| chr4:184762791 | G | A | 43 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0022 others(40): Show |
45 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1522-268C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762791 | |||||||
| chr4:184762856 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1521+311C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762856 | |||||||
| chr4:184762974 | G | T | 1 | a0001c0010t0001g0302 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1521+193C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184762974 | |||||||
| chr4:184763093 | T | C | 25 | a0001c0001t0004g0048 a0001c0001t0004g0138 a0001c0001t0004g0139 others(22): Show |
25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1521+74A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184763093 | |||||||
| chr4:184763123 | C | A | 1 | a0001c0007t0002g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1521+44G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 16/20 | chr4 | 184763123 | |||||||
| chr4:184763840 | A | G | 2 | a0001c0005t0012g0149 a0001c0005t0014g0151 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1433-585T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184763840 | |||||||
| chr4:184763946 | CTG | C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1433-693_1433-692d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184763946 | |||||||
| chr4:184763989 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1433-734T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184763989 | |||||||
| chr4:184764091 | T | G | 1 | a0003c0012t0002g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1432+762A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764091 | |||||||
| chr4:184764109 | C | T | 1 | a0001c0006t0002g0037 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1432+744G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764109 | |||||||
| chr4:184764203 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1432+650G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764203 | |||||||
| chr4:184764226 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1432+627A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764226 | |||||||
| chr4:184764453 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
168 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.1432+400T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764453 | |||||||
| chr4:184764568 | T | C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432+285A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764568 | |||||||
| chr4:184764651 | C | T | 2 | a0001c0001t0005g0321 a0001c0001t0005g0322 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1432+202G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 15/20 | chr4 | 184764651 | |||||||
| chr4:184765498 | G | A | 90 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0007 others(87): Show |
96 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1359+393C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765498 | |||||||
| chr4:184765513 | G | A | 6 | a0001c0003t0003g0141 a0001c0003t0003g0142 a0001c0003t0003g0310 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1359+378C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765513 | |||||||
| chr4:184765634 | T | C | 5 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0023 others(2): Show |
6 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1359+257A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765634 | |||||||
| chr4:184765653 | C | T | 1 | a0001c0002t0002g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1359+238G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765653 | |||||||
| chr4:184765702 | C | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.1359+189G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765702 | |||||||
| chr4:184765735 | T | C | 15 | a0001c0001t0002g0088 a0001c0001t0002g0148 a0001c0001t0002g0158 others(12): Show |
15 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1359+156A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765735 | |||||||
| chr4:184765794 | A | AAC | 9 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0023 others(6): Show |
10 | HG00735.hp1 HG01358.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1359+95_1359+96dup others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 14/20 | chr4 | 184765794 | |||||||
| chr4:184766079 | C | T | 77 | a0001c0001t0002g0007 a0001c0001t0002g0034 a0001c0001t0002g0093 others(74): Show |
81 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1264-93G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766079 | |||||||
| chr4:184766201 | A | G | 15 | a0001c0001t0002g0088 a0001c0001t0002g0148 a0001c0001t0002g0158 others(12): Show |
15 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264-215T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766201 | |||||||
| chr4:184766219 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
186 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.1264-233T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766219 | |||||||
| chr4:184766366 | C | T | 12 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0001g0345 others(9): Show |
14 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.1263+256G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766366 | |||||||
| chr4:184766430 | A | G | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1263+192T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766430 | |||||||
| chr4:184766533 | A | C | 80 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0022 others(77): Show |
86 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1263+89T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766533 | |||||||
| chr4:184766590 | C | T | 2 | a0001c0001t0001g0345 a0001c0001t0002g0344 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1263+32G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 13/20 | chr4 | 184766590 | |||||||
| chr4:184766764 | G | A | 1 | a0001c0003t0003g0264 | 1 | HG03239.hp2 | splice_region_variant&intron_variant | LOW | c.1129-8C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184766764 | |||||||
| chr4:184766898 | G | T | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1129-142C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184766898 | |||||||
| chr4:184766938 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1129-182C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184766938 | |||||||
| chr4:184766994 | T | C | 5 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0023 others(2): Show |
6 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-238A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184766994 | |||||||
| chr4:184767118 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1129-362G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767118 | |||||||
| chr4:184767139 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1129-383C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767139 | |||||||
| chr4:184767283 | C | CA | 77 | a0001c0001t0001g0225 a0001c0001t0002g0007 a0001c0001t0002g0022 others(74): Show |
82 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1129-528dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767283 | |||||||
| chr4:184767283 | CA | C | 30 | a0001c0001t0001g0166 a0001c0001t0001g0247 a0001c0001t0002g0092 others(27): Show |
30 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1129-528delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767283 | |||||||
| chr4:184767447 | A | C | 1 | a0001c0002t0002g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1129-691T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767447 | |||||||
| chr4:184767494 | G | A | 1 | a0001c0001t0002g0099 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1129-738C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767494 | |||||||
| chr4:184767497 | G | A | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1129-741C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767497 | |||||||
| chr4:184767600 | C | T | 40 | a0001c0003t0003g0006 a0001c0003t0003g0012 a0001c0003t0003g0018 others(37): Show |
44 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1128+716G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767600 | |||||||
| chr4:184767825 | G | A | 1 | a0001c0001t0004g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1128+491C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184767825 | |||||||
| chr4:184768013 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
178 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.1128+303C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184768013 | |||||||
| chr4:184768065 | G | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0155 a0001c0001t0002g0214 |
4 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128+251C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184768065 | |||||||
| chr4:184768195 | C | T | 4 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128+121G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184768195 | |||||||
| chr4:184768221 | G | T | 2 | a0001c0001t0001g0325 a0001c0001t0001g0327 |
2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1128+95C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 12/20 | chr4 | 184768221 | |||||||
| chr4:184768678 | C | A | 4 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.994-228G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768678 | |||||||
| chr4:184768711 | G | A | 4 | a0001c0004t0001g0047 a0001c0004t0001g0268 a0001c0004t0001g0269 others(1): Show |
4 | HG00609.hp2 HG02040.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.994-261C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768711 | |||||||
| chr4:184768730 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.994-280C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768730 | |||||||
| chr4:184768737 | A | G | 1 | a0001c0003t0003g0329 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.994-287T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768737 | |||||||
| chr4:184768798 | G | A | 26 | a0001c0001t0003g0343 a0001c0001t0004g0048 a0001c0001t0004g0138 others(23): Show |
26 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.994-348C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768798 | |||||||
| chr4:184768833 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
178 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.994-383C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184768833 | |||||||
| chr4:184769070 | A | AAT | 20 | a0001c0001t0001g0320 a0001c0001t0002g0014 a0001c0001t0002g0158 others(17): Show |
22 | HG00733.hp2 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.994-622_994-621dup others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | A | AATAT | 47 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0023 others(44): Show |
50 | HG00099.hp1 HG00558.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.994-624_994-621dup others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | A | AATATAT | 13 | a0001c0002t0002g0005 a0001c0002t0002g0049 a0001c0002t0002g0054 others(10): Show |
14 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.994-626_994-621dup others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | A | AATATATA others(1): Show |
10 | a0001c0002t0002g0036 a0001c0002t0002g0057 a0001c0002t0002g0064 others(7): Show |
10 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.994-628_994-621dup others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | A | AATATATA others(3): Show |
2 | a0001c0002t0002g0058 a0001c0002t0002g0060 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.994-630_994-621dup others(10): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | A | AATATATA others(7): Show |
1 | a0001c0001t0002g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.994-634_994-621dup others(14): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | A | AATATATA others(19): Show |
1 | a0001c0001t0002g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.994-621_994-620ins others(26): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | A | AATATATA others(21): Show |
1 | a0001c0001t0002g0016 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.994-621_994-620ins others(28): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | AAT | A | 17 | a0001c0001t0002g0088 a0001c0001t0002g0148 a0001c0001t0002g0167 others(14): Show |
17 | HG01884.hp1 HG01891.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.994-622_994-621del others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | AATAT | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
212 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(209): Show |
intron_variant | MODIFIER | c.994-624_994-621del others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769070 | AATATAT | A | 47 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0001g0345 others(44): Show |
52 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.994-626_994-621del others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769070 | |||||||
| chr4:184769112 | A | G | 6 | a0001c0001t0002g0040 a0001c0001t0002g0073 a0001c0001t0002g0086 others(3): Show |
6 | HG02602.hp1 HG02602.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-662T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769112 | |||||||
| chr4:184769177 | C | T | 31 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(28): Show |
31 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.994-727G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769177 | |||||||
| chr4:184769249 | G | A | 1 | a0001c0006t0002g0201 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.994-799C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769249 | |||||||
| chr4:184769285 | A | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(11): Show |
15 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.994-835T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769285 | |||||||
| chr4:184769438 | G | A | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.993+961C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769438 | |||||||
| chr4:184769447 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
178 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.993+952T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769447 | |||||||
| chr4:184769859 | A | G | 6 | a0001c0001t0002g0040 a0001c0001t0002g0073 a0001c0001t0002g0086 others(3): Show |
6 | HG02602.hp1 HG02602.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+540T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184769859 | |||||||
| chr4:184770002 | G | A | 1 | a0001c0005t0012g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.993+397C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184770002 | |||||||
| chr4:184770051 | T | C | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.993+348A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184770051 | |||||||
| chr4:184770260 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.993+139T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184770260 | |||||||
| chr4:184770361 | T | C | 26 | a0001c0001t0001g0320 a0001c0001t0002g0014 a0001c0001t0002g0088 others(23): Show |
27 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.993+38A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 11/20 | chr4 | 184770361 | |||||||
| chr4:184770541 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0292 a0001c0001t0001g0293 |
4 | NA18943.hp1 NA18964.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-65G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770541 | |||||||
| chr4:184770654 | T | C | 1 | a0001c0003t0003g0256 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.916-178A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770654 | |||||||
| chr4:184770719 | A | T | 1 | a0001c0005t0003g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.916-243T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770719 | |||||||
| chr4:184770729 | G | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-253C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770729 | |||||||
| chr4:184770734 | C | T | 40 | a0001c0003t0003g0006 a0001c0003t0003g0012 a0001c0003t0003g0018 others(37): Show |
44 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.916-258G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770734 | |||||||
| chr4:184770809 | C | A | 2 | a0001c0001t0001g0345 a0001c0001t0002g0344 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.916-333G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770809 | |||||||
| chr4:184770824 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.916-348T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184770824 | |||||||
| chr4:184771007 | C | G | 1 | a0001c0002t0002g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.916-531G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771007 | |||||||
| chr4:184771279 | C | T | 2 | a0001c0001t0001g0345 a0001c0001t0002g0344 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.916-803G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771279 | |||||||
| chr4:184771300 | C | A | 2 | a0001c0001t0001g0345 a0001c0001t0002g0344 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.916-824G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771300 | |||||||
| chr4:184771352 | A | G | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-876T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771352 | |||||||
| chr4:184771600 | G | C | 1 | a0001c0003t0003g0329 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.916-1124C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771600 | |||||||
| chr4:184771665 | A | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0214 |
3 | HG01358.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.916-1189T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771665 | |||||||
| chr4:184771700 | T | C | 1 | a0001c0002t0007g0347 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916-1224A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771700 | |||||||
| chr4:184771838 | GC | G | 31 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(28): Show |
31 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.915+1242delG | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771838 | |||||||
| chr4:184771931 | T | C | 2 | a0001c0002t0002g0156 a0001c0002t0002g0220 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.915+1150A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184771931 | |||||||
| chr4:184772200 | T | A | 2 | a0001c0002t0002g0053 a0001c0002t0002g0055 |
2 | HG00558.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.915+881A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772200 | |||||||
| chr4:184772303 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0155 a0001c0001t0002g0214 |
4 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+778G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772303 | |||||||
| chr4:184772401 | T | C | 19 | a0001c0001t0001g0320 a0001c0001t0002g0014 a0001c0001t0002g0159 others(16): Show |
20 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+680A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772401 | |||||||
| chr4:184772479 | C | T | 2 | a0001c0001t0001g0345 a0001c0001t0002g0344 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.915+602G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772479 | |||||||
| chr4:184772482 | T | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.915+599A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772482 | |||||||
| chr4:184772563 | C | T | 1 | a0001c0005t0003g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.915+518G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772563 | |||||||
| chr4:184772800 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
176 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.915+281C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772800 | |||||||
| chr4:184772896 | C | T | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.915+185G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772896 | |||||||
| chr4:184772911 | T | A | 6 | a0001c0001t0002g0040 a0001c0001t0002g0073 a0001c0001t0002g0086 others(3): Show |
6 | HG02602.hp1 HG02602.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+170A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772911 | |||||||
| chr4:184772962 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+119A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 10/20 | chr4 | 184772962 | |||||||
| chr4:184773263 | G | A | 1 | a0001c0002t0002g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.842-109C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773263 | |||||||
| chr4:184773399 | T | G | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.842-245A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773399 | |||||||
| chr4:184773535 | C | G | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.841+128G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773535 | |||||||
| chr4:184773543 | G | A | 40 | a0001c0003t0003g0006 a0001c0003t0003g0012 a0001c0003t0003g0018 others(37): Show |
44 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.841+120C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773543 | |||||||
| chr4:184773622 | A | G | 26 | a0001c0001t0003g0343 a0001c0001t0004g0048 a0001c0001t0004g0138 others(23): Show |
26 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.841+41T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773622 | |||||||
| chr4:184773623 | T | C | 4 | a0001c0001t0002g0088 a0001c0001t0002g0148 a0001c0001t0002g0185 others(1): Show |
4 | HG01975.hp2 HG02572.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+40A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773623 | |||||||
| chr4:184773636 | T | C | 1 | a0001c0002t0002g0055 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.841+27A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 9/20 | chr4 | 184773636 | |||||||
| chr4:184773723 | T | TA | 32 | a0001c0001t0001g0320 a0001c0001t0002g0014 a0001c0001t0002g0040 others(29): Show |
33 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.790-10dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 8/20 | chr4 | 184773723 | |||||||
| chr4:184773981 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.757-106G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184773981 | |||||||
| chr4:184774109 | T | C | 81 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0031 others(78): Show |
84 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.757-234A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774109 | |||||||
| chr4:184774170 | G | A | 41 | a0001c0003t0003g0006 a0001c0003t0003g0012 a0001c0003t0003g0018 others(38): Show |
45 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.757-295C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774170 | |||||||
| chr4:184774264 | T | C | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.757-389A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774264 | |||||||
| chr4:184774407 | A | C | 11 | a0001c0001t0001g0320 a0001c0001t0002g0014 a0001c0001t0002g0159 others(8): Show |
12 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.757-532T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774407 | |||||||
| chr4:184774487 | T | C | 3 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0342 |
3 | NA18939.hp1 NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.757-612A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774487 | |||||||
| chr4:184774583 | C | T | 4 | a0001c0001t0004g0048 a0001c0001t0004g0138 a0001c0001t0004g0139 others(1): Show |
4 | HG00735.hp1 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-708G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774583 | |||||||
| chr4:184774623 | A | G | 2 | a0001c0001t0001g0325 a0001c0001t0001g0327 |
2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.757-748T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774623 | |||||||
| chr4:184774740 | C | T | 2 | a0001c0001t0005g0321 a0001c0001t0005g0322 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.757-865G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774740 | |||||||
| chr4:184774791 | ACATT | A | 81 | a0001c0001t0001g0333 a0001c0001t0002g0007 a0001c0001t0002g0022 others(78): Show |
86 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.757-920_757-917del others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184774791 | |||||||
| chr4:184775094 | G | A | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.757-1219C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775094 | |||||||
| chr4:184775143 | A | T | 2 | a0001c0001t0001g0345 a0001c0001t0002g0344 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.757-1268T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775143 | |||||||
| chr4:184775471 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0298 |
3 | HG01361.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.756+1013T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775471 | |||||||
| chr4:184775537 | C | T | 31 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(28): Show |
31 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.756+947G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775537 | |||||||
| chr4:184775551 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756+933G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775551 | |||||||
| chr4:184775579 | G | A | 34 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(31): Show |
34 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.756+905C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775579 | |||||||
| chr4:184775585 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.756+899A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775585 | |||||||
| chr4:184775702 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.756+782G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775702 | |||||||
| chr4:184775843 | C | T | 6 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(3): Show |
6 | HG01099.hp1 HG01167.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.756+641G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775843 | |||||||
| chr4:184775894 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0085 a0001c0001t0001g0089 others(2): Show |
5 | HG00597.hp1 HG02523.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.756+590C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184775894 | |||||||
| chr4:184776035 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.756+449G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776035 | |||||||
| chr4:184776067 | C | T | 1 | a0001c0004t0001g0270 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.756+417G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776067 | |||||||
| chr4:184776132 | T | C | 1 | a0001c0004t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.756+352A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776132 | |||||||
| chr4:184776222 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.756+262C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776222 | |||||||
| chr4:184776260 | T | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | NA18955.hp2 NA19063.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+224A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776260 | |||||||
| chr4:184776287 | G | T | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(360): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.756+197C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776287 | |||||||
| chr4:184776327 | C | A | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.756+157G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776327 | |||||||
| chr4:184776364 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.756+120G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776364 | |||||||
| chr4:184776370 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.756+114G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776370 | |||||||
| chr4:184776376 | GCC | G | 3 | a0001c0002t0002g0005 a0001c0002t0002g0049 a0001c0002t0002g0078 |
4 | HG00741.hp1 HG02027.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+106_756+107del others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776376 | |||||||
| chr4:184776387 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.756+97C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776387 | |||||||
| chr4:184776422 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.756+62G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 7/20 | chr4 | 184776422 | |||||||
| chr4:184776812 | G | A | 2 | a0001c0003t0003g0018 a0001c0003t0003g0309 |
3 | HG00741.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.577+72C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 6/20 | chr4 | 184776812 | |||||||
| chr4:184776853 | C | T | 2 | a0001c0002t0002g0216 a0001c0002t0002g0217 |
2 | NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.577+31G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 6/20 | chr4 | 184776853 | |||||||
| chr4:184777029 | T | G | 3 | a0001c0001t0002g0016 a0001c0001t0002g0155 a0001c0001t0002g0214 |
4 | HG01358.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-46A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777029 | |||||||
| chr4:184777186 | G | T | 2 | a0001c0001t0004g0048 a0001c0001t0004g0206 |
2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.478-203C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777186 | |||||||
| chr4:184777291 | A | G | 15 | a0001c0001t0003g0343 a0001c0001t0004g0048 a0001c0001t0004g0138 others(12): Show |
15 | HG00735.hp1 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.478-308T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777291 | |||||||
| chr4:184777497 | G | A | 1 | a0001c0002t0002g0314 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.478-514C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777497 | |||||||
| chr4:184777557 | G | C | 26 | a0001c0001t0001g0320 a0001c0001t0002g0014 a0001c0001t0002g0088 others(23): Show |
27 | HG01884.hp1 HG01975.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.478-574C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777557 | |||||||
| chr4:184777577 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.478-594T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777577 | |||||||
| chr4:184777781 | A | AAG | 25 | a0001c0001t0003g0343 a0001c0001t0004g0048 a0001c0001t0004g0138 others(22): Show |
25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.478-800_478-799dup others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777781 | |||||||
| chr4:184777903 | C | G | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.478-920G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184777903 | |||||||
| chr4:184778020 | CAA | C | 79 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0023 others(76): Show |
84 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.478-1039_478-1038d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778020 | |||||||
| chr4:184778134 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.478-1151A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778134 | |||||||
| chr4:184778225 | T | C | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.478-1242A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778225 | |||||||
| chr4:184778246 | T | A | 5 | a0001c0006t0002g0037 a0001c0006t0002g0087 a0001c0006t0002g0201 others(2): Show |
5 | NA18973.hp2 NA18979.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-1263A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778246 | |||||||
| chr4:184778478 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.478-1495G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778478 | |||||||
| chr4:184778479 | G | A | 31 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(28): Show |
31 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.478-1496C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778479 | |||||||
| chr4:184778744 | T | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
182 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.477+1588A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778744 | |||||||
| chr4:184778764 | T | C | 11 | a0001c0001t0004g0335 a0001c0001t0004g0337 a0001c0001t0004g0338 others(8): Show |
11 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.477+1568A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778764 | |||||||
| chr4:184778873 | G | T | 3 | a0001c0003t0003g0006 a0001c0003t0003g0026 a0001c0003t0003g0097 |
4 | HG00544.hp1 NA18965.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+1459C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778873 | |||||||
| chr4:184778884 | G | A | 14 | a0001c0003t0003g0006 a0001c0003t0003g0021 a0001c0003t0003g0026 others(11): Show |
16 | HG00544.hp1 HG02015.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.477+1448C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778884 | |||||||
| chr4:184778943 | T | TA | 42 | a0001c0001t0001g0212 a0001c0002t0002g0314 a0001c0003t0003g0006 others(39): Show |
46 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.477+1388dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184778943 | |||||||
| chr4:184779050 | T | C | 1 | a0001c0003t0003g0012 | 2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.477+1282A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779050 | |||||||
| chr4:184779073 | T | G | 1 | a0001c0001t0001g0359 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.477+1259A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779073 | |||||||
| chr4:184779075 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.477+1257A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779075 | |||||||
| chr4:184779110 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.477+1222A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779110 | |||||||
| chr4:184779122 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.477+1210G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779122 | |||||||
| chr4:184779175 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.477+1157C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779175 | |||||||
| chr4:184779223 | A | G | 2 | a0001c0001t0004g0355 a0001c0001t0004g0356 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.477+1109T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779223 | |||||||
| chr4:184779323 | G | T | 6 | a0001c0001t0005g0321 a0001c0001t0005g0322 a0001c0002t0002g0197 others(3): Show |
6 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.477+1009C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779323 | |||||||
| chr4:184779327 | T | C | 6 | a0001c0001t0005g0321 a0001c0001t0005g0322 a0001c0002t0002g0197 others(3): Show |
6 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.477+1005A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779327 | |||||||
| chr4:184779355 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.477+977C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779355 | |||||||
| chr4:184779386 | C | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0085 a0001c0001t0001g0089 others(3): Show |
7 | HG00597.hp1 HG02523.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+946G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779386 | |||||||
| chr4:184779400 | A | G | 1 | a0001c0001t0001g0361 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.477+932T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779400 | |||||||
| chr4:184779615 | G | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.477+717C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779615 | |||||||
| chr4:184779622 | T | G | 147 | a0001c0001t0001g0112 a0001c0001t0001g0116 a0001c0001t0001g0119 others(144): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.477+710A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779622 | |||||||
| chr4:184779812 | A | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
159 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.477+520T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779812 | |||||||
| chr4:184779842 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0086 |
2 | NA18944.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.477+490G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779842 | |||||||
| chr4:184779866 | T | A | 1 | a0001c0001t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.477+466A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779866 | |||||||
| chr4:184779874 | C | CT | 15 | a0001c0001t0001g0212 a0001c0001t0004g0335 a0001c0001t0004g0337 others(12): Show |
15 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.477+457dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779874 | |||||||
| chr4:184779874 | CT | C | 7 | a0001c0001t0001g0224 a0001c0001t0002g0040 a0001c0001t0002g0073 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+457delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184779874 | |||||||
| chr4:184780181 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.477+151C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184780181 | |||||||
| chr4:184780289 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.477+43C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 5/20 | chr4 | 184780289 | |||||||
| chr4:184780466 | T | C | 41 | a0001c0003t0003g0006 a0001c0003t0003g0012 a0001c0003t0003g0018 others(38): Show |
45 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.376-33A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780466 | |||||||
| chr4:184780478 | T | A | 3 | a0001c0002t0002g0069 a0001c0002t0002g0107 a0001c0002t0002g0110 |
3 | HG02109.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.376-45A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780478 | |||||||
| chr4:184780659 | A | C | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(360): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.376-226T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780659 | |||||||
| chr4:184780868 | T | TAG | 10 | a0001c0001t0001g0027 a0001c0001t0001g0051 a0001c0001t0001g0082 others(7): Show |
10 | HG02071.hp2 NA18949.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.376-436_376-435ins others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780868 | |||||||
| chr4:184780912 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.376-479C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780912 | |||||||
| chr4:184780976 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0255 a0001c0001t0001g0287 |
3 | HG00280.hp2 HG00438.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.376-543G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184780976 | |||||||
| chr4:184781016 | A | T | 92 | a0001c0001t0001g0112 a0001c0001t0001g0212 a0001c0001t0001g0215 others(89): Show |
99 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.376-583T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781016 | |||||||
| chr4:184781018 | CACTT | C | 92 | a0001c0001t0001g0112 a0001c0001t0001g0212 a0001c0001t0001g0215 others(89): Show |
99 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.376-589_376-586del others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781018 | |||||||
| chr4:184781229 | CAA | C | 7 | a0001c0002t0002g0057 a0001c0002t0002g0078 a0001c0002t0002g0218 others(4): Show |
7 | HG02027.hp2 HG03516.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.376-798_376-797del others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | |||||||
| chr4:184781229 | CAAA | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0051 others(131): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.376-799_376-797del others(3): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | |||||||
| chr4:184781229 | CAAAA | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(207): Show |
223 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(220): Show |
intron_variant | MODIFIER | c.376-800_376-797del others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | |||||||
| chr4:184781229 | CAAAAA | C | 9 | a0001c0001t0001g0052 a0001c0001t0001g0260 a0001c0001t0001g0274 others(6): Show |
10 | HG01257.hp2 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.376-801_376-797del others(5): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | |||||||
| chr4:184781229 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0002g0177 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.376-807_376-797del others(11): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781229 | |||||||
| chr4:184781460 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376-1027A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781460 | |||||||
| chr4:184781481 | T | A | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-1048A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781481 | |||||||
| chr4:184781536 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.376-1103T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781536 | |||||||
| chr4:184781554 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.376-1121T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781554 | |||||||
| chr4:184781797 | G | A | 1 | a0001c0003t0003g0308 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.376-1364C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781797 | |||||||
| chr4:184781921 | T | C | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-1488A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781921 | |||||||
| chr4:184781950 | A | C | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.376-1517T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781950 | |||||||
| chr4:184781953 | A | G | 1 | a0001c0002t0002g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.376-1520T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781953 | |||||||
| chr4:184781979 | A | G | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(353): Show |
380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.376-1546T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184781979 | |||||||
| chr4:184782160 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.376-1727T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782160 | |||||||
| chr4:184782201 | C | T | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(360): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.375+1726G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782201 | |||||||
| chr4:184782264 | T | TA | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
202 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.375+1662dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782264 | |||||||
| chr4:184782264 | T | TAAA | 90 | a0001c0001t0001g0112 a0001c0001t0001g0212 a0001c0001t0001g0215 others(87): Show |
97 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.375+1660_375+1662d others(5): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782264 | |||||||
| chr4:184782446 | A | AT | 5 | a0001c0003t0003g0029 a0001c0003t0003g0232 a0001c0003t0003g0277 others(2): Show |
5 | HG02083.hp2 HG03831.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+1480dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782446 | |||||||
| chr4:184782493 | T | C | 1 | a0001c0004t0001g0267 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.375+1434A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782493 | |||||||
| chr4:184782513 | A | T | 2 | a0001c0001t0003g0343 a0001c0001t0004g0203 |
2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.375+1414T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782513 | |||||||
| chr4:184782591 | C | G | 2 | a0001c0002t0002g0216 a0001c0002t0002g0217 |
2 | NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.375+1336G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782591 | |||||||
| chr4:184782628 | T | C | 1 | a0001c0002t0002g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.375+1299A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782628 | |||||||
| chr4:184782998 | T | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0181 a0001c0002t0002g0346 others(1): Show |
5 | HG01891.hp2 HG02717.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+929A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184782998 | |||||||
| chr4:184783022 | G | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.375+905C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783022 | |||||||
| chr4:184783045 | G | A | 27 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(24): Show |
27 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.375+882C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783045 | |||||||
| chr4:184783111 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.375+816G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783111 | |||||||
| chr4:184783258 | T | C | 135 | a0001c0001t0001g0112 a0001c0001t0001g0212 a0001c0001t0001g0215 others(132): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.375+669A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783258 | |||||||
| chr4:184783280 | G | A | 10 | a0001c0001t0001g0112 a0001c0002t0002g0039 a0001c0002t0002g0109 others(7): Show |
10 | HG00099.hp1 HG01099.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.375+647C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783280 | |||||||
| chr4:184783294 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.375+633A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783294 | |||||||
| chr4:184783436 | T | C | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(360): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.375+491A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783436 | |||||||
| chr4:184783546 | C | T | 92 | a0001c0001t0001g0112 a0001c0001t0001g0212 a0001c0001t0001g0215 others(89): Show |
99 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.375+381G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783546 | |||||||
| chr4:184783652 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
161 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.375+275C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783652 | |||||||
| chr4:184783804 | G | A | 1 | a0001c0003t0003g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.375+123C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783804 | |||||||
| chr4:184783851 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.375+76G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783851 | |||||||
| chr4:184783852 | G | A | 92 | a0001c0001t0001g0112 a0001c0001t0001g0212 a0001c0001t0001g0215 others(89): Show |
99 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.375+75C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | 184783852 | |||||||
| chr4:184784027 | G | A | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.311-36C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784027 | |||||||
| chr4:184784052 | T | A | 1 | a0001c0002t0002g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.311-61A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784052 | |||||||
| chr4:184784240 | T | C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-249A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784240 | |||||||
| chr4:184784267 | G | C | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.311-276C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784267 | |||||||
| chr4:184784271 | CCTCTTT | C | 5 | a0001c0003t0003g0006 a0001c0003t0003g0026 a0001c0003t0003g0081 others(2): Show |
6 | HG00544.hp1 NA18947.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-286_311-281del others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784271 | |||||||
| chr4:184784287 | C | T | 5 | a0001c0003t0003g0006 a0001c0003t0003g0026 a0001c0003t0003g0081 others(2): Show |
6 | HG00544.hp1 NA18947.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-296G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784287 | |||||||
| chr4:184784497 | G | A | 25 | a0001c0001t0001g0046 a0001c0001t0004g0048 a0001c0001t0004g0138 others(22): Show |
25 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.311-506C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784497 | |||||||
| chr4:184784812 | G | T | 1 | a0001c0002t0002g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.311-821C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784812 | |||||||
| chr4:184784953 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.311-962A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784953 | |||||||
| chr4:184784997 | T | C | 95 | a0001c0001t0001g0112 a0001c0001t0001g0134 a0001c0001t0001g0137 others(92): Show |
102 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.311-1006A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784997 | |||||||
| chr4:184784999 | C | T | 92 | a0001c0001t0001g0112 a0001c0001t0001g0134 a0001c0001t0001g0137 others(89): Show |
98 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.311-1008G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184784999 | |||||||
| chr4:184785343 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0315 |
2 | NA18949.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.311-1352T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785343 | |||||||
| chr4:184785360 | C | T | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-1369G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785360 | |||||||
| chr4:184785596 | TGGGCGG | T | 8 | a0001c0001t0001g0102 a0001c0001t0001g0350 a0001c0002t0002g0110 others(5): Show |
8 | HG01261.hp2 HG02622.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.311-1611_311-1606d others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785596 | |||||||
| chr4:184785600 | C | CCGGG | 5 | a0001c0001t0002g0365 a0001c0003t0003g0018 a0001c0003t0003g0305 others(2): Show |
5 | HG01168.hp2 HG01257.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-1610_311-1609i others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | C | CCGGGG | 10 | a0001c0001t0002g0158 a0001c0003t0003g0006 a0001c0003t0003g0012 others(7): Show |
12 | HG01070.hp2 HG02486.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.311-1610_311-1609i others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | C | CCGGGGG | 13 | a0001c0001t0002g0364 a0001c0003t0003g0021 a0001c0003t0003g0094 others(10): Show |
13 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.311-1610_311-1609i others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | C | CCGGGGGG | 11 | a0001c0003t0003g0018 a0001c0003t0003g0029 a0001c0003t0003g0097 others(8): Show |
11 | HG00544.hp1 HG00741.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-1610_311-1609i others(9): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | C | CCGGGGGG others(4): Show |
1 | a0001c0003t0003g0311 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.311-1610_311-1609i others(13): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | CGGGGGCG | C | 32 | a0001c0001t0001g0031 a0001c0001t0001g0106 a0001c0001t0001g0134 others(29): Show |
33 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.311-1616_311-1610d others(9): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | CGGGGGCG others(1): Show |
C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(141): Show |
151 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.311-1617_311-1610d others(10): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | CGGGGGCG others(2): Show |
C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0044 others(50): Show |
56 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.311-1618_311-1610d others(11): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | CGGGGGCG others(3): Show |
C | 6 | a0001c0001t0001g0137 a0001c0001t0002g0222 a0001c0002t0002g0053 others(3): Show |
6 | HG00558.hp2 HG01081.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-1619_311-1610d others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | CGGGGGCG others(5): Show |
C | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.311-1621_311-1610d others(14): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785600 | CGGGGGCG others(6): Show |
C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(18): Show |
22 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.311-1622_311-1610d others(15): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785600 | |||||||
| chr4:184785605 | GC | G | 3 | a0001c0001t0001g0169 a0001c0001t0002g0040 a0001c0001t0002g0099 |
3 | HG02602.hp2 HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.311-1615delG | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785605 | |||||||
| chr4:184785606 | C | G | 73 | a0001c0001t0001g0046 a0001c0001t0002g0158 a0001c0001t0002g0159 others(70): Show |
77 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.311-1615G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785606 | |||||||
| chr4:184785607 | G | T | 2 | a0001c0001t0001g0169 a0001c0001t0002g0061 |
2 | NA18952.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.311-1616C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785607 | |||||||
| chr4:184785609 | G | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0166 others(2): Show |
7 | HG02280.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.311-1618C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785609 | |||||||
| chr4:184785613 | G | T | 1 | a0001c0002t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311-1622C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785613 | |||||||
| chr4:184785614 | G | GGGGGGGG others(3): Show |
1 | a0001c0001t0004g0206 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.311-1624_311-1623i others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785614 | |||||||
| chr4:184785614 | G | T | 1 | a0001c0002t0002g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.311-1623C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785614 | |||||||
| chr4:184785615 | G | A | 47 | a0001c0001t0002g0040 a0001c0001t0002g0073 a0001c0001t0002g0086 others(44): Show |
51 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.311-1624C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785615 | |||||||
| chr4:184785615 | G | GGGGGGGG others(3): Show |
2 | a0001c0001t0004g0144 a0001c0001t0004g0354 |
2 | HG01106.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.311-1625_311-1624i others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785615 | |||||||
| chr4:184785615 | G | GGGGGGGG others(8): Show |
1 | a0001c0001t0004g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.311-1625_311-1624i others(17): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785615 | |||||||
| chr4:184785616 | G | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0132 others(2): Show |
5 | HG01891.hp2 HG03516.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-1625C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785616 | |||||||
| chr4:184785617 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.311-1626C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785617 | |||||||
| chr4:184785622 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(237): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.311-1631T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785622 | |||||||
| chr4:184785683 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.311-1692C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785683 | |||||||
| chr4:184785713 | T | A | 2 | a0001c0002t0002g0156 a0001c0002t0002g0220 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.311-1722A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184785713 | |||||||
| chr4:184786005 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.311-2014C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786005 | |||||||
| chr4:184786119 | C | T | 1 | a0001c0001t0011g0066 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.311-2128G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786119 | |||||||
| chr4:184786191 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.311-2200C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786191 | |||||||
| chr4:184786305 | G | T | 22 | a0001c0002t0002g0011 a0001c0002t0002g0036 a0001c0002t0002g0038 others(19): Show |
23 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.310+2312C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786305 | |||||||
| chr4:184786349 | A | G | 1 | a0001c0002t0002g0179 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.310+2268T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786349 | |||||||
| chr4:184786418 | G | GCA | 3 | a0001c0001t0001g0015 a0001c0001t0001g0186 a0001c0005t0012g0149 |
4 | HG01074.hp1 HG01109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.310+2197_310+2198d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | |||||||
| chr4:184786418 | G | GCACGCAC others(9): Show |
2 | a0001c0002t0002g0156 a0001c0002t0002g0220 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.310+2198_310+2199i others(18): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | |||||||
| chr4:184786418 | GCA | G | 36 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0112 others(33): Show |
36 | HG00558.hp1 HG00735.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.310+2197_310+2198d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | |||||||
| chr4:184786418 | GCACA | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(208): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.310+2195_310+2198d others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | |||||||
| chr4:184786418 | GCACACA | G | 11 | a0001c0001t0004g0335 a0001c0001t0004g0337 a0001c0001t0004g0338 others(8): Show |
11 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.310+2193_310+2198d others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | |||||||
| chr4:184786418 | GCACACAC others(3): Show |
G | 15 | a0001c0001t0001g0046 a0001c0001t0004g0048 a0001c0001t0004g0138 others(12): Show |
15 | HG00642.hp2 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.310+2189_310+2198d others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | |||||||
| chr4:184786418 | GCACACAC others(5): Show |
G | 5 | a0001c0001t0002g0040 a0001c0001t0002g0073 a0001c0001t0002g0086 others(2): Show |
5 | HG02602.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+2187_310+2198d others(14): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | |||||||
| chr4:184786418 | GCACACAC others(11): Show |
G | 1 | a0001c0002t0002g0179 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.310+2181_310+2198d others(20): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786418 | |||||||
| chr4:184786420 | A | ACG | 14 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(11): Show |
14 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.310+2196_310+2197i others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786420 | |||||||
| chr4:184786422 | A | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0166 others(49): Show |
58 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.310+2195T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786422 | |||||||
| chr4:184786424 | A | G | 26 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0112 others(23): Show |
26 | HG00558.hp1 HG00735.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.310+2193T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786424 | |||||||
| chr4:184786425 | C | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0359 a0001c0001t0001g0360 |
3 | HG00597.hp2 HG02165.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.310+2192G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786425 | |||||||
| chr4:184786426 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(211): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.310+2191T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786426 | |||||||
| chr4:184786427 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0166 others(3): Show |
8 | HG02280.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.310+2190G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786427 | |||||||
| chr4:184786428 | A | G | 15 | a0001c0001t0002g0016 a0001c0001t0002g0214 a0001c0001t0004g0335 others(12): Show |
16 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.310+2189T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786428 | |||||||
| chr4:184786430 | A | G | 4 | a0001c0001t0001g0252 a0001c0002t0002g0114 a0001c0002t0002g0115 others(1): Show |
4 | HG00438.hp1 NA18960.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+2187T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786430 | |||||||
| chr4:184786432 | A | G | 15 | a0001c0001t0001g0046 a0001c0001t0004g0048 a0001c0001t0004g0138 others(12): Show |
15 | HG00642.hp2 HG00735.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.310+2185T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786432 | |||||||
| chr4:184786434 | A | G | 5 | a0001c0001t0002g0040 a0001c0001t0002g0073 a0001c0001t0002g0086 others(2): Show |
5 | HG02602.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+2183T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786434 | |||||||
| chr4:184786440 | A | G | 1 | a0001c0002t0002g0179 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.310+2177T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786440 | |||||||
| chr4:184786456 | ACACT | A | 38 | a0001c0001t0003g0343 a0001c0001t0004g0203 a0001c0003t0003g0006 others(35): Show |
42 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.310+2157_310+2160d others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786456 | |||||||
| chr4:184786458 | ACT | A | 4 | a0001c0001t0002g0158 a0001c0001t0002g0364 a0001c0001t0002g0365 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+2157_310+2158d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786458 | |||||||
| chr4:184786460 | T | A | 1 | a0001c0003t0003g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.310+2157A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786460 | |||||||
| chr4:184786553 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.310+2064A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786553 | |||||||
| chr4:184786596 | A | G | 6 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0001g0225 others(3): Show |
7 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+2021T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786596 | |||||||
| chr4:184786692 | C | CTT | 42 | a0001c0001t0002g0158 a0001c0001t0002g0364 a0001c0001t0002g0365 others(39): Show |
46 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.310+1923_310+1924d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786692 | |||||||
| chr4:184786692 | CT | C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0133 a0001c0001t0001g0260 others(10): Show |
14 | HG01069.hp1 HG01257.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.310+1924delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786692 | |||||||
| chr4:184786692 | CTT | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(218): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.310+1923_310+1924d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786692 | |||||||
| chr4:184786716 | C | T | 2 | a0001c0008t0004g0297 a0001c0008t0004g0304 |
2 | HG00639.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.310+1901G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786716 | |||||||
| chr4:184786725 | G | A | 22 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(19): Show |
23 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.310+1892C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184786725 | |||||||
| chr4:184787025 | C | T | 33 | a0001c0001t0001g0134 a0001c0001t0002g0007 a0001c0001t0002g0034 others(30): Show |
36 | HG00438.hp2 HG00558.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.310+1592G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787025 | |||||||
| chr4:184787026 | C | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.310+1591G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787026 | |||||||
| chr4:184787265 | G | A | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+1352C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787265 | |||||||
| chr4:184787274 | G | A | 4 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+1343C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787274 | |||||||
| chr4:184787319 | C | T | 6 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0001g0225 others(3): Show |
7 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+1298G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787319 | |||||||
| chr4:184787330 | A | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0166 others(3): Show |
8 | HG02280.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.310+1287T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787330 | |||||||
| chr4:184787441 | A | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.310+1176T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787441 | |||||||
| chr4:184787482 | G | A | 72 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0042 others(69): Show |
74 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.310+1135C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787482 | |||||||
| chr4:184787596 | A | G | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.310+1021T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787596 | |||||||
| chr4:184787601 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.310+1016G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787601 | |||||||
| chr4:184787613 | C | T | 21 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(18): Show |
22 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.310+1004G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787613 | |||||||
| chr4:184787653 | T | C | 38 | a0001c0001t0001g0046 a0001c0001t0002g0040 a0001c0001t0002g0073 others(35): Show |
38 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.310+964A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787653 | |||||||
| chr4:184787724 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.310+893G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787724 | |||||||
| chr4:184787757 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(280): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.310+860T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787757 | |||||||
| chr4:184787867 | G | GA | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(280): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.310+749dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787867 | |||||||
| chr4:184787904 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0129 |
4 | HG02683.hp1 HG02698.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+713T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184787904 | |||||||
| chr4:184788043 | G | C | 1 | a0001c0001t0001g0293 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.310+574C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788043 | |||||||
| chr4:184788203 | T | G | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+414A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788203 | |||||||
| chr4:184788219 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.310+398T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788219 | |||||||
| chr4:184788394 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.310+223C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788394 | |||||||
| chr4:184788502 | G | A | 1 | a0001c0002t0002g0177 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.310+115C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788502 | |||||||
| chr4:184788524 | G | A | 2 | a0001c0002t0002g0156 a0001c0002t0002g0220 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.310+93C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3/20 | chr4 | 184788524 | |||||||
| chr4:184788737 | A | G | 8 | a0001c0001t0004g0337 a0001c0001t0004g0338 a0001c0001t0004g0351 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.196-6T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184788737 | |||||||
| chr4:184788875 | T | C | 2 | a0001c0001t0003g0343 a0001c0001t0004g0203 |
2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.196-144A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184788875 | |||||||
| chr4:184789546 | T | C | 1 | a0001c0001t0004g0301 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.196-815A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789546 | |||||||
| chr4:184789651 | T | C | 8 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(5): Show |
8 | HG02615.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-920A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789651 | |||||||
| chr4:184789684 | T | C | 37 | a0001c0003t0003g0006 a0001c0003t0003g0012 a0001c0003t0003g0018 others(34): Show |
41 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.196-953A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789684 | |||||||
| chr4:184789705 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(236): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.196-974C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789705 | |||||||
| chr4:184789883 | CT | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(330): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.196-1153delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789883 | |||||||
| chr4:184789883 | CTT | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0136 others(24): Show |
29 | HG00609.hp1 HG01123.hp2 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-1154_196-1153d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789883 | |||||||
| chr4:184789944 | T | G | 1 | a0001c0001t0002g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.196-1213A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789944 | |||||||
| chr4:184789959 | G | A | 1 | a0001c0006t0002g0201 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.196-1228C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184789959 | |||||||
| chr4:184790063 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196-1332T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790063 | |||||||
| chr4:184790068 | T | C | 43 | a0001c0001t0002g0158 a0001c0001t0002g0364 a0001c0001t0002g0365 others(40): Show |
47 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.196-1337A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790068 | |||||||
| chr4:184790081 | T | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196-1350A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790081 | |||||||
| chr4:184790113 | G | A | 2 | a0001c0001t0002g0195 a0001c0002t0002g0105 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.196-1382C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790113 | |||||||
| chr4:184790398 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.196-1667A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790398 | |||||||
| chr4:184790520 | G | A | 2 | a0001c0001t0002g0364 a0001c0001t0002g0365 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.196-1789C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790520 | |||||||
| chr4:184790848 | T | TAGC | 26 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(23): Show |
26 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-2120_196-2118d others(5): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790848 | |||||||
| chr4:184790942 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.196-2211C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790942 | |||||||
| chr4:184790980 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0166 others(48): Show |
54 | HG01099.hp1 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.196-2249C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184790980 | |||||||
| chr4:184791000 | T | A | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.196-2269A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791000 | |||||||
| chr4:184791061 | T | C | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.196-2330A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791061 | |||||||
| chr4:184791142 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.196-2411A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791142 | |||||||
| chr4:184791173 | T | C | 42 | a0001c0001t0002g0158 a0001c0001t0002g0364 a0001c0001t0002g0365 others(39): Show |
46 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.196-2442A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791173 | |||||||
| chr4:184791443 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.196-2712G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791443 | |||||||
| chr4:184791454 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.196-2723C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791454 | |||||||
| chr4:184791455 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.196-2724G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791455 | |||||||
| chr4:184791525 | G | C | 36 | a0001c0002t0002g0276 a0001c0003t0003g0006 a0001c0003t0003g0012 others(33): Show |
40 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.196-2794C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791525 | |||||||
| chr4:184791616 | A | G | 3 | a0001c0001t0001g0294 a0001c0001t0001g0313 a0001c0001t0001g0336 |
3 | HG00735.hp2 HG01081.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.196-2885T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791616 | |||||||
| chr4:184791701 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0212 a0001c0001t0001g0215 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-2970C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184791701 | |||||||
| chr4:184792163 | T | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(17): Show |
22 | HG02280.hp2 HG02602.hp1 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-3432A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792163 | |||||||
| chr4:184792185 | A | G | 1 | a0001c0005t0012g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196-3454T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792185 | |||||||
| chr4:184792195 | T | C | 43 | a0001c0001t0001g0230 a0001c0001t0001g0235 a0001c0001t0001g0296 others(40): Show |
47 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.196-3464A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792195 | |||||||
| chr4:184792255 | C | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(16): Show |
21 | HG02280.hp2 HG02602.hp1 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.196-3524G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792255 | |||||||
| chr4:184792414 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
185 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(182): Show |
intron_variant | MODIFIER | c.196-3683T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792414 | |||||||
| chr4:184792441 | A | AT | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-3711dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792441 | |||||||
| chr4:184792454 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-3723C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792454 | |||||||
| chr4:184792484 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
215 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(212): Show |
intron_variant | MODIFIER | c.196-3753T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792484 | |||||||
| chr4:184792524 | C | T | 1 | a0001c0005t0003g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196-3793G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792524 | |||||||
| chr4:184792525 | G | A | 1 | a0001c0002t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196-3794C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792525 | |||||||
| chr4:184792586 | G | A | 1 | a0001c0001t0004g0354 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.196-3855C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792586 | |||||||
| chr4:184792761 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(92): Show |
107 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.196-4030C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792761 | |||||||
| chr4:184792769 | A | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(36): Show |
42 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.196-4038T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792769 | |||||||
| chr4:184792878 | G | A | 3 | a0001c0002t0002g0058 a0001c0002t0002g0060 a0001c0002t0004g0059 |
3 | HG00642.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.196-4147C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792878 | |||||||
| chr4:184792947 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-4216T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792947 | |||||||
| chr4:184792976 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196-4245T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184792976 | |||||||
| chr4:184793135 | G | T | 42 | a0001c0001t0001g0046 a0001c0001t0001g0172 a0001c0001t0001g0173 others(39): Show |
42 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.196-4404C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793135 | |||||||
| chr4:184793165 | C | CTTTAATG | 2 | a0001c0001t0001g0020 a0001c0001t0001g0298 |
3 | HG01361.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.196-4441_196-4435d others(9): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793165 | |||||||
| chr4:184793194 | TA | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(166): Show |
187 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.196-4464delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793194 | |||||||
| chr4:184793194 | TAA | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0082 a0001c0001t0001g0182 others(6): Show |
10 | HG01256.hp1 HG01361.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-4465_196-4464d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793194 | |||||||
| chr4:184793244 | G | A | 12 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(9): Show |
12 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-4513C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793244 | |||||||
| chr4:184793247 | G | A | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.196-4516C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793247 | |||||||
| chr4:184793425 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(9): Show |
14 | HG02280.hp2 HG02602.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-4694G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793425 | |||||||
| chr4:184793540 | G | A | 2 | a0001c0001t0001g0345 a0001c0001t0002g0344 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.196-4809C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793540 | |||||||
| chr4:184793541 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.196-4810T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793541 | |||||||
| chr4:184793649 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.196-4918C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793649 | |||||||
| chr4:184793751 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.196-5020G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793751 | |||||||
| chr4:184793802 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(140): Show |
156 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(153): Show |
intron_variant | MODIFIER | c.196-5071G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793802 | |||||||
| chr4:184793819 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
8 | HG02280.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-5088G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184793819 | |||||||
| chr4:184794013 | A | G | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-5282T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794013 | |||||||
| chr4:184794111 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5380G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794111 | |||||||
| chr4:184794130 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.196-5399C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794130 | |||||||
| chr4:184794132 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5401C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794132 | |||||||
| chr4:184794170 | T | C | 44 | a0001c0001t0001g0046 a0001c0001t0001g0172 a0001c0001t0001g0173 others(41): Show |
44 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.196-5439A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794170 | |||||||
| chr4:184794203 | A | AAC | 45 | a0001c0001t0001g0046 a0001c0001t0001g0172 a0001c0001t0001g0173 others(42): Show |
45 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.196-5473_196-5472i others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794203 | |||||||
| chr4:184794297 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.196-5566G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794297 | |||||||
| chr4:184794342 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196-5611T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794342 | |||||||
| chr4:184794376 | A | T | 1 | a0001c0008t0004g0297 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.196-5645T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794376 | |||||||
| chr4:184794397 | A | G | 1 | a0001c0004t0001g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.196-5666T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794397 | |||||||
| chr4:184794451 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.196-5720G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794451 | |||||||
| chr4:184794452 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5721C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794452 | |||||||
| chr4:184794531 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5800A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794531 | |||||||
| chr4:184794532 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5801C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794532 | |||||||
| chr4:184794535 | A | G | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5804T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794535 | |||||||
| chr4:184794584 | C | G | 1 | a0001c0001t0002g0366 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196-5853G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794584 | |||||||
| chr4:184794698 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-5967C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794698 | |||||||
| chr4:184794747 | A | G | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6016T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794747 | |||||||
| chr4:184794903 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6172A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794903 | |||||||
| chr4:184794915 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.196-6184G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794915 | |||||||
| chr4:184794922 | C | CCAAT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(140): Show |
156 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(153): Show |
intron_variant | MODIFIER | c.196-6192_196-6191i others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794922 | |||||||
| chr4:184794936 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6205C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794936 | |||||||
| chr4:184794946 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6215C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184794946 | |||||||
| chr4:184795078 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6347A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795078 | |||||||
| chr4:184795108 | G | A | 1 | a0001c0003t0003g0012 | 2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.196-6377C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795108 | |||||||
| chr4:184795114 | A | AT | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6384dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795114 | |||||||
| chr4:184795138 | T | C | 2 | a0001c0001t0004g0355 a0001c0001t0004g0356 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.196-6407A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795138 | |||||||
| chr4:184795335 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6604G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795335 | |||||||
| chr4:184795347 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196-6616C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795347 | |||||||
| chr4:184795452 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6721G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795452 | |||||||
| chr4:184795463 | T | G | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6732A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795463 | |||||||
| chr4:184795499 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-6768G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795499 | |||||||
| chr4:184795783 | T | C | 23 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(20): Show |
23 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.196-7052A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795783 | |||||||
| chr4:184795875 | G | C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-7144C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795875 | |||||||
| chr4:184795930 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.196-7199A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184795930 | |||||||
| chr4:184796091 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+7229C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796091 | |||||||
| chr4:184796148 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+7172A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796148 | |||||||
| chr4:184796195 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.195+7125C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796195 | |||||||
| chr4:184796243 | G | A | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0274 others(1): Show |
4 | HG00609.hp1 HG01074.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+7077C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796243 | |||||||
| chr4:184796323 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6997A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796323 | |||||||
| chr4:184796469 | C | G | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6851G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796469 | |||||||
| chr4:184796474 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6846G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796474 | |||||||
| chr4:184796568 | T | C | 45 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(42): Show |
49 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.195+6752A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796568 | |||||||
| chr4:184796590 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6730G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796590 | |||||||
| chr4:184796605 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6715A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796605 | |||||||
| chr4:184796649 | T | G | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6671A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796649 | |||||||
| chr4:184796955 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+6365A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796955 | |||||||
| chr4:184796978 | A | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
157 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(154): Show |
intron_variant | MODIFIER | c.195+6342T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184796978 | |||||||
| chr4:184797067 | C | T | 34 | a0001c0001t0001g0046 a0001c0001t0002g0159 a0001c0001t0002g0160 others(31): Show |
34 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.195+6253G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797067 | |||||||
| chr4:184797077 | A | G | 1 | a0001c0001t0002g0344 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.195+6243T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797077 | |||||||
| chr4:184797146 | A | C | 39 | a0001c0001t0001g0046 a0001c0001t0001g0171 a0001c0001t0001g0210 others(36): Show |
40 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.195+6174T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797146 | |||||||
| chr4:184797160 | CCGCTCA | C | 39 | a0001c0001t0001g0046 a0001c0001t0001g0171 a0001c0001t0001g0210 others(36): Show |
40 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.195+6154_195+6159d others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797160 | |||||||
| chr4:184797167 | C | G | 39 | a0001c0001t0001g0046 a0001c0001t0001g0171 a0001c0001t0001g0210 others(36): Show |
40 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.195+6153G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797167 | |||||||
| chr4:184797303 | C | T | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+6017G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797303 | |||||||
| chr4:184797332 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5988A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797332 | |||||||
| chr4:184797339 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5981A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797339 | |||||||
| chr4:184797365 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5955C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797365 | |||||||
| chr4:184797378 | G | A | 1 | a0001c0005t0003g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.195+5942C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797378 | |||||||
| chr4:184797429 | C | G | 1 | a0001c0003t0003g0309 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.195+5891G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797429 | |||||||
| chr4:184797452 | C | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5868G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797452 | |||||||
| chr4:184797504 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.195+5816G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797504 | |||||||
| chr4:184797573 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
165 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(162): Show |
intron_variant | MODIFIER | c.195+5747C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797573 | |||||||
| chr4:184797599 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.195+5721C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797599 | |||||||
| chr4:184797622 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5698A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797622 | |||||||
| chr4:184797764 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0085 a0001c0001t0001g0089 |
3 | HG00597.hp1 HG02523.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.195+5556G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797764 | |||||||
| chr4:184797816 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.195+5504A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797816 | |||||||
| chr4:184797915 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.195+5405G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797915 | |||||||
| chr4:184797918 | C | T | 1 | a0001c0002t0002g0107 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.195+5402G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797918 | |||||||
| chr4:184797970 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5350C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797970 | |||||||
| chr4:184797972 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5348G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797972 | |||||||
| chr4:184797997 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+5323A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184797997 | |||||||
| chr4:184798021 | A | T | 1 | a0001c0001t0002g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+5299T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798021 | |||||||
| chr4:184798037 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.195+5283C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798037 | |||||||
| chr4:184798085 | G | T | 1 | a0001c0002t0002g0076 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.195+5235C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798085 | |||||||
| chr4:184798103 | G | A | 10 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+5217C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798103 | |||||||
| chr4:184798166 | A | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0292 others(2): Show |
6 | NA18941.hp1 NA18943.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+5154T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798166 | |||||||
| chr4:184798306 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.195+5014G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798306 | |||||||
| chr4:184798453 | C | T | 2 | a0001c0002t0002g0276 a0001c0003t0003g0263 |
2 | HG00280.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.195+4867G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798453 | |||||||
| chr4:184798545 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.195+4775C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184798545 | |||||||
| chr4:184799061 | TC | T | 10 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+4258delG | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799061 | |||||||
| chr4:184799085 | C | A | 1 | a0001c0002t0002g0035 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.195+4235G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799085 | |||||||
| chr4:184799086 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(115): Show |
130 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(127): Show |
intron_variant | MODIFIER | c.195+4234G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799086 | |||||||
| chr4:184799102 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
171 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(168): Show |
intron_variant | MODIFIER | c.195+4218A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799102 | |||||||
| chr4:184799116 | C | CT | 25 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(22): Show |
25 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.195+4203dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799116 | |||||||
| chr4:184799116 | CT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
108 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.195+4203delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799116 | |||||||
| chr4:184799116 | CTT | C | 17 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0171 others(14): Show |
18 | HG02280.hp1 HG02615.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+4202_195+4203d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799116 | |||||||
| chr4:184799150 | G | T | 12 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(9): Show |
12 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.195+4170C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799150 | |||||||
| chr4:184799155 | G | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(98): Show |
112 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(109): Show |
intron_variant | MODIFIER | c.195+4165C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799155 | |||||||
| chr4:184799168 | G | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+4152C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799168 | |||||||
| chr4:184799274 | G | A | 10 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+4046C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799274 | |||||||
| chr4:184799305 | C | T | 4 | a0001c0001t0001g0234 a0001c0003t0003g0021 a0001c0003t0003g0233 others(1): Show |
5 | NA18966.hp2 NA18994.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+4015G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799305 | |||||||
| chr4:184799318 | T | C | 9 | a0001c0001t0004g0337 a0001c0001t0004g0338 a0001c0001t0004g0351 others(6): Show |
9 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+4002A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799318 | |||||||
| chr4:184799489 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.195+3831G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799489 | |||||||
| chr4:184799689 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.195+3631T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184799689 | |||||||
| chr4:184800138 | T | C | 1 | a0001c0001t0001g0360 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.195+3182A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800138 | |||||||
| chr4:184800144 | T | C | 4 | a0001c0001t0001g0042 a0001c0003t0003g0310 a0001c0003t0003g0311 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+3176A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800144 | |||||||
| chr4:184800198 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(88): Show |
102 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.195+3122C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800198 | |||||||
| chr4:184800216 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
165 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(162): Show |
intron_variant | MODIFIER | c.195+3104C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800216 | |||||||
| chr4:184800579 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(88): Show |
102 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.195+2741A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800579 | |||||||
| chr4:184800646 | C | T | 1 | a0001c0001t0004g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.195+2674G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800646 | |||||||
| chr4:184800721 | A | G | 1 | a0001c0003t0003g0308 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.195+2599T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184800721 | |||||||
| chr4:184801107 | C | T | 5 | a0001c0001t0001g0204 a0001c0001t0001g0248 a0001c0001t0001g0253 others(2): Show |
5 | NA18747.hp1 NA18949.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+2213G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801107 | |||||||
| chr4:184801133 | G | GT | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(88): Show |
102 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.195+2186_195+2187i others(3): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801133 | |||||||
| chr4:184801293 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+2027A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801293 | |||||||
| chr4:184801342 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.195+1978A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801342 | |||||||
| chr4:184801474 | T | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0051 a0001c0001t0001g0100 others(4): Show |
7 | HG02071.hp2 NA18962.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+1846A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801474 | |||||||
| chr4:184801565 | G | C | 1 | a0001c0002t0002g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.195+1755C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801565 | |||||||
| chr4:184801572 | T | C | 5 | a0001c0001t0001g0275 a0001c0002t0002g0008 a0001c0002t0002g0070 others(2): Show |
6 | NA18612.hp2 NA18962.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+1748A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801572 | |||||||
| chr4:184801688 | A | G | 9 | a0001c0001t0001g0027 a0001c0001t0001g0051 a0001c0001t0001g0100 others(6): Show |
9 | HG02071.hp2 NA18950.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+1632T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801688 | |||||||
| chr4:184801692 | C | G | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+1628G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801692 | |||||||
| chr4:184801737 | C | G | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.195+1583G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801737 | |||||||
| chr4:184801766 | C | T | 10 | a0001c0001t0001g0134 a0001c0001t0002g0007 a0001c0001t0002g0034 others(7): Show |
11 | NA18939.hp1 NA18951.hp1 NA18969.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+1554G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801766 | |||||||
| chr4:184801844 | C | G | 5 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(2): Show |
6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+1476G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184801844 | |||||||
| chr4:184802052 | GA | G | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.195+1267delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802052 | |||||||
| chr4:184802556 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.195+764C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802556 | |||||||
| chr4:184802557 | C | T | 39 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0235 others(36): Show |
42 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.195+763G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802557 | |||||||
| chr4:184802618 | C | A | 7 | a0001c0001t0002g0222 a0001c0001t0002g0231 a0001c0002t0002g0017 others(4): Show |
8 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.195+702G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802618 | |||||||
| chr4:184802657 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+663G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802657 | |||||||
| chr4:184802688 | G | A | 1 | a0001c0004t0001g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.195+632C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802688 | |||||||
| chr4:184802688 | G | T | 9 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(6): Show |
9 | HG02615.hp1 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+632C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802688 | |||||||
| chr4:184802767 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0198 |
2 | HG02071.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.195+553G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802767 | |||||||
| chr4:184802778 | G | A | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0001t0004g0147 |
3 | HG01123.hp2 HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.195+542C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802778 | |||||||
| chr4:184802855 | C | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
12 | HG02280.hp2 HG02602.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.195+465G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802855 | |||||||
| chr4:184802927 | G | A | 1 | a0001c0001t0004g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.195+393C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802927 | |||||||
| chr4:184802936 | C | A | 1 | a0001c0001t0002g0332 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.195+384G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802936 | |||||||
| chr4:184802945 | A | G | 17 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(14): Show |
18 | HG01081.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+375T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184802945 | |||||||
| chr4:184803060 | G | A | 1 | a0001c0002t0002g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.195+260C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184803060 | |||||||
| chr4:184803101 | C | T | 1 | a0001c0003t0003g0309 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.195+219G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184803101 | |||||||
| chr4:184803303 | C | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0298 |
3 | HG01361.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.195+17G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 2/20 | chr4 | 184803303 | |||||||
| chr4:184803594 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0207 a0001c0002t0002g0105 others(7): Show |
10 | HG01928.hp2 NA18953.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-48G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184803594 | |||||||
| chr4:184803607 | C | A | 9 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-61G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184803607 | |||||||
| chr4:184803944 | C | G | 1 | a0001c0003t0003g0308 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-32-398G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184803944 | |||||||
| chr4:184803994 | C | T | 10 | a0001c0001t0001g0134 a0001c0001t0002g0007 a0001c0001t0002g0034 others(7): Show |
11 | NA18939.hp1 NA18951.hp1 NA18969.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-448G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184803994 | |||||||
| chr4:184804000 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-32-454C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804000 | |||||||
| chr4:184804255 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32-709A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804255 | |||||||
| chr4:184804262 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
217 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(214): Show |
intron_variant | MODIFIER | c.-32-716T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804262 | |||||||
| chr4:184804342 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(159): Show |
178 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(175): Show |
intron_variant | MODIFIER | c.-32-796T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804342 | |||||||
| chr4:184804366 | G | A | 9 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-820C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804366 | |||||||
| chr4:184804530 | G | A | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-984C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804530 | |||||||
| chr4:184804587 | GA | G | 11 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0002g0013 others(8): Show |
12 | HG01891.hp1 HG01993.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32-1042delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804587 | |||||||
| chr4:184804587 | GAA | G | 11 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(8): Show |
11 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-1043_-32-1042d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804587 | |||||||
| chr4:184804674 | C | A | 1 | a0001c0006t0002g0087 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-32-1128G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804674 | |||||||
| chr4:184804709 | A | T | 1 | a0001c0001t0001g0259 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-32-1163T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804709 | |||||||
| chr4:184804790 | C | A | 2 | a0001c0001t0002g0191 a0001c0001t0002g0194 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-32-1244G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804790 | |||||||
| chr4:184804968 | G | A | 1 | a0001c0001t0004g0143 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-32-1422C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184804968 | |||||||
| chr4:184805070 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-32-1524G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805070 | |||||||
| chr4:184805113 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0327 |
2 | HG02027.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-32-1567A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805113 | |||||||
| chr4:184805267 | T | A | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-1721A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805267 | |||||||
| chr4:184805380 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0113 a0001c0001t0001g0127 |
3 | NA18978.hp1 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-32-1834A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805380 | |||||||
| chr4:184805394 | C | T | 159 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0041 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-32-1848G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805394 | |||||||
| chr4:184805395 | TCACA | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0028 others(7): Show |
15 | HG00544.hp2 NA18612.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.-32-1853_-32-1850d others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805395 | |||||||
| chr4:184805507 | C | G | 1 | a0001c0001t0002g0022 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-32-1961G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805507 | |||||||
| chr4:184805524 | C | T | 1 | a0001c0002t0002g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-32-1978G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805524 | |||||||
| chr4:184805760 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-2214A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805760 | |||||||
| chr4:184805847 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
8 | HG02280.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-2301C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805847 | |||||||
| chr4:184805956 | C | G | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-2410G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805956 | |||||||
| chr4:184805987 | C | G | 1 | a0001c0001t0002g0330 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-32-2441G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184805987 | |||||||
| chr4:184806593 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-32-3047C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184806593 | |||||||
| chr4:184806685 | T | A | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-3139A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184806685 | |||||||
| chr4:184807570 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-32-4024G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807570 | |||||||
| chr4:184807657 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(120): Show |
136 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(133): Show |
intron_variant | MODIFIER | c.-32-4111T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807657 | |||||||
| chr4:184807685 | T | C | 65 | a0001c0001t0001g0041 a0001c0001t0001g0134 a0001c0001t0001g0207 others(62): Show |
68 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-32-4139A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807685 | |||||||
| chr4:184807767 | AAAAGC | A | 11 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-4226_-32-4222d others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807767 | |||||||
| chr4:184807836 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(10): Show |
14 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32-4290T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807836 | |||||||
| chr4:184807869 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-32-4323G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184807869 | |||||||
| chr4:184808084 | G | T | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-32-4538C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808084 | |||||||
| chr4:184808202 | A | G | 1 | a0001c0002t0002g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-32-4656T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808202 | |||||||
| chr4:184808240 | T | TAC | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(95): Show |
110 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.-32-4696_-32-4695d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808240 | |||||||
| chr4:184808733 | C | A | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-5187G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808733 | |||||||
| chr4:184808894 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-32-5348C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808894 | |||||||
| chr4:184808920 | C | T | 1 | a0001c0002t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32-5374G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808920 | |||||||
| chr4:184808980 | T | C | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-5434A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184808980 | |||||||
| chr4:184809038 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-32-5492G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809038 | |||||||
| chr4:184809145 | G | A | 36 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0235 others(33): Show |
39 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-32-5599C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809145 | |||||||
| chr4:184809485 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(5): Show |
10 | HG02280.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-5939A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809485 | |||||||
| chr4:184809531 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-32-5985T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809531 | |||||||
| chr4:184809596 | T | C | 22 | a0001c0001t0001g0046 a0001c0001t0003g0343 a0001c0001t0004g0048 others(19): Show |
22 | HG00735.hp1 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-6050A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809596 | |||||||
| chr4:184809636 | C | CA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(93): Show |
108 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(105): Show |
intron_variant | MODIFIER | c.-32-6091dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809636 | |||||||
| chr4:184809775 | G | A | 9 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-6229C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809775 | |||||||
| chr4:184809800 | A | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(183): Show |
202 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.-32-6254T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809800 | |||||||
| chr4:184809946 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-32-6400A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184809946 | |||||||
| chr4:184810049 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-32-6503A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810049 | |||||||
| chr4:184810157 | C | T | 5 | a0001c0001t0002g0093 a0001c0004t0001g0004 a0001c0004t0001g0246 others(2): Show |
7 | HG00738.hp1 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-6611G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810157 | |||||||
| chr4:184810275 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-32-6729C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810275 | |||||||
| chr4:184810288 | G | A | 34 | a0001c0001t0001g0084 a0001c0001t0001g0230 a0001c0001t0001g0234 others(31): Show |
37 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-32-6742C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810288 | |||||||
| chr4:184810311 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-32-6765G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810311 | |||||||
| chr4:184810429 | C | T | 36 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0235 others(33): Show |
39 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-32-6883G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810429 | |||||||
| chr4:184810669 | C | T | 1 | a0001c0002t0002g0314 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-32-7123G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810669 | |||||||
| chr4:184810708 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0129 |
4 | HG02683.hp1 HG02698.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-7162C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810708 | |||||||
| chr4:184810721 | C | CGGATA | 10 | a0001c0001t0001g0320 a0001c0001t0002g0159 a0001c0001t0002g0160 others(7): Show |
10 | HG02615.hp1 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-7180_-32-7176d others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810721 | |||||||
| chr4:184810786 | G | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0136 others(69): Show |
78 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-32-7240C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810786 | |||||||
| chr4:184810934 | G | C | 12 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0001g0212 others(9): Show |
13 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-7388C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810934 | |||||||
| chr4:184810976 | G | C | 12 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(9): Show |
12 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-7430C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184810976 | |||||||
| chr4:184811019 | G | C | 1 | a0001c0001t0001g0250 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-32-7473C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811019 | |||||||
| chr4:184811067 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-32-7521A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811067 | |||||||
| chr4:184811147 | C | T | 1 | a0001c0002t0002g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-32-7601G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811147 | |||||||
| chr4:184811148 | G | A | 1 | a0001c0002t0002g0064 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-32-7602C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811148 | |||||||
| chr4:184811171 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(81): Show |
95 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.-32-7625A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811171 | |||||||
| chr4:184811177 | C | T | 7 | a0001c0001t0004g0337 a0001c0001t0004g0338 a0001c0001t0004g0351 others(4): Show |
7 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-7631G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811177 | |||||||
| chr4:184811209 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0027 others(57): Show |
67 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-32-7663G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811209 | |||||||
| chr4:184811213 | A | G | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-7667T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811213 | |||||||
| chr4:184811220 | C | T | 21 | a0001c0001t0001g0009 a0001c0001t0001g0135 a0001c0001t0001g0294 others(18): Show |
24 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32-7674G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811220 | |||||||
| chr4:184811221 | A | G | 34 | a0001c0001t0001g0009 a0001c0001t0001g0135 a0001c0001t0001g0171 others(31): Show |
38 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.-32-7675T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811221 | |||||||
| chr4:184811232 | C | G | 1 | a0001c0002t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-32-7686G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811232 | |||||||
| chr4:184811233 | G | C | 3 | a0001c0001t0001g0025 a0001c0002t0002g0005 a0001c0003t0003g0094 |
4 | NA18967.hp2 NA18971.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-7687C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811233 | |||||||
| chr4:184811254 | A | G | 14 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0187 others(11): Show |
14 | HG01099.hp1 HG02486.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32-7708T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811254 | |||||||
| chr4:184811264 | A | G | 7 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0001g0345 others(4): Show |
7 | HG02486.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-7718T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811264 | |||||||
| chr4:184811265 | C | T | 42 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0182 others(39): Show |
44 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.-32-7719G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811265 | |||||||
| chr4:184811266 | G | T | 1 | a0001c0002t0002g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-32-7720C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811266 | |||||||
| chr4:184811269 | T | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0294 a0001c0001t0001g0296 others(6): Show |
10 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-7723A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811269 | |||||||
| chr4:184811275 | AT | A | 11 | a0001c0001t0001g0169 a0001c0001t0001g0224 a0001c0001t0002g0014 others(8): Show |
12 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-7730delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811275 | |||||||
| chr4:184811304 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-32-7758C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811304 | |||||||
| chr4:184811313 | C | T | 2 | a0001c0002t0002g0011 a0001c0008t0004g0297 |
3 | HG00639.hp2 NA18975.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-32-7767G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811313 | |||||||
| chr4:184811314 | G | A | 4 | a0001c0001t0001g0319 a0001c0002t0002g0197 a0001c0002t0002g0240 others(1): Show |
4 | HG01361.hp1 HG02976.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-7768C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811314 | |||||||
| chr4:184811319 | G | A | 10 | a0001c0001t0001g0100 a0001c0001t0001g0116 a0001c0001t0001g0117 others(7): Show |
11 | HG00639.hp2 HG02071.hp2 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-7773C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811319 | |||||||
| chr4:184811319 | G | C | 1 | a0001c0010t0001g0302 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-32-7773C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811319 | |||||||
| chr4:184811324 | G | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0298 a0001c0001t0004g0144 others(4): Show |
8 | HG01106.hp2 HG01109.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32-7778C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811324 | |||||||
| chr4:184811326 | A | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0298 a0001c0001t0004g0138 others(15): Show |
19 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.-32-7780T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811326 | |||||||
| chr4:184811333 | C | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0298 others(18): Show |
22 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32-7787G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811333 | |||||||
| chr4:184811334 | G | A | 1 | a0001c0001t0002g0363 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-32-7788C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811334 | |||||||
| chr4:184811334 | G | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0298 others(18): Show |
22 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32-7788C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811334 | |||||||
| chr4:184811341 | C | T | 2 | a0001c0007t0002g0152 a0001c0007t0002g0153 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-7795G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811341 | |||||||
| chr4:184811354 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-32-7808A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811354 | |||||||
| chr4:184811363 | T | C | 42 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0025 others(39): Show |
44 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.-32-7817A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811363 | |||||||
| chr4:184811363 | TGGCCTCC others(8898): Show |
T | 1 | a0001c0002t0002g0197 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-33+5648_-32-7818d others(2): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811363 | |||||||
| chr4:184811370 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-32-7824G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811370 | |||||||
| chr4:184811391 | T | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(60): Show |
72 | HG00544.hp2 HG00673.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.-32-7845A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811391 | |||||||
| chr4:184811397 | C | T | 1 | a0001c0002t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32-7851G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811397 | |||||||
| chr4:184811401 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-32-7855G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811401 | |||||||
| chr4:184811402 | G | A | 7 | a0001c0001t0001g0208 a0001c0002t0002g0035 a0001c0002t0002g0121 others(4): Show |
8 | HG00544.hp1 HG02015.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-7856C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811402 | |||||||
| chr4:184811403 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-32-7857G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811403 | |||||||
| chr4:184811404 | G | A | 17 | a0001c0001t0001g0313 a0001c0001t0004g0138 a0001c0001t0004g0139 others(14): Show |
17 | HG00735.hp1 HG01069.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-32-7858C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811404 | |||||||
| chr4:184811407 | C | T | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-7861G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811407 | |||||||
| chr4:184811408 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
286 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(283): Show |
intron_variant | MODIFIER | c.-32-7862T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811408 | |||||||
| chr4:184811486 | A | G | 2 | a0001c0001t0001g0345 a0001c0001t0002g0344 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-32-7940T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811486 | |||||||
| chr4:184811504 | A | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0019 others(144): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-32-7958T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184811504 | |||||||
| chr4:184812030 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-8484G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812030 | |||||||
| chr4:184812054 | C | T | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.-32-8508G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812054 | |||||||
| chr4:184812182 | T | C | 2 | a0001c0001t0005g0321 a0001c0001t0005g0322 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-32-8636A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812182 | |||||||
| chr4:184812454 | C | T | 1 | a0001c0001t0002g0344 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-32-8908G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812454 | |||||||
| chr4:184812455 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(128): Show |
141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-32-8909C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812455 | |||||||
| chr4:184812470 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-8924G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812470 | |||||||
| chr4:184812572 | GCT | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-9028_-32-9027d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812572 | |||||||
| chr4:184812588 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-32-9042A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812588 | |||||||
| chr4:184812637 | A | T | 5 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0002g0221 others(2): Show |
5 | HG02486.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-9091T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812637 | |||||||
| chr4:184812816 | C | T | 6 | a0001c0001t0004g0337 a0001c0001t0004g0338 a0001c0001t0004g0351 others(3): Show |
6 | HG01358.hp1 HG01433.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-9270G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184812816 | |||||||
| chr4:184813009 | A | G | 18 | a0001c0001t0004g0138 a0001c0001t0004g0143 a0001c0001t0004g0144 others(15): Show |
18 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-32-9463T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813009 | |||||||
| chr4:184813029 | C | CAAACA | 8 | a0001c0001t0001g0169 a0001c0001t0001g0224 a0001c0001t0001g0230 others(5): Show |
8 | HG02027.hp1 HG02071.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-9488_-32-9484d others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813029 | |||||||
| chr4:184813128 | G | A | 1 | a0001c0002t0002g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-32-9582C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813128 | |||||||
| chr4:184813130 | T | C | 1 | a0001c0003t0003g0326 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-32-9584A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813130 | |||||||
| chr4:184813159 | T | A | 1 | a0001c0003t0003g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-32-9613A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813159 | |||||||
| chr4:184813208 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-9662C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813208 | |||||||
| chr4:184813221 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-9675C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813221 | |||||||
| chr4:184813430 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-32-9884C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813430 | |||||||
| chr4:184813473 | A | G | 1 | a0001c0003t0003g0264 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-32-9927T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813473 | |||||||
| chr4:184813519 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG02818.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-32-9973G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813519 | |||||||
| chr4:184813559 | G | C | 1 | a0001c0001t0001g0327 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-32-10013C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813559 | |||||||
| chr4:184813578 | C | T | 1 | a0001c0002t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-32-10032G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813578 | |||||||
| chr4:184813579 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0002g0013 a0001c0001t0002g0170 |
4 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-10033C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813579 | |||||||
| chr4:184813631 | C | T | 1 | a0001c0003t0003g0263 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-32-10085G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813631 | |||||||
| chr4:184813632 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-32-10086C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813632 | |||||||
| chr4:184813637 | G | C | 1 | a0001c0001t0001g0327 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-32-10091C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813637 | |||||||
| chr4:184813644 | C | T | 1 | a0001c0003t0003g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-32-10098G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813644 | |||||||
| chr4:184813718 | A | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-10172T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813718 | |||||||
| chr4:184813727 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-32-10181G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813727 | |||||||
| chr4:184813900 | G | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(126): Show |
139 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-32-10354C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813900 | |||||||
| chr4:184813980 | A | G | 1 | a0001c0005t0003g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32-10434T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813980 | |||||||
| chr4:184813988 | A | G | 19 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(16): Show |
20 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-32-10442T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184813988 | |||||||
| chr4:184814061 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-32-10515G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814061 | |||||||
| chr4:184814168 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-32-10622C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814168 | |||||||
| chr4:184814190 | C | G | 1 | a0001c0003t0003g0256 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-32-10644G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814190 | |||||||
| chr4:184814208 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0131 others(1): Show |
4 | NA18955.hp2 NA19010.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-10662T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814208 | |||||||
| chr4:184814209 | T | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0131 others(1): Show |
4 | NA18955.hp2 NA19010.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-10663A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814209 | |||||||
| chr4:184814256 | T | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
318 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.-32-10710A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814256 | |||||||
| chr4:184814277 | C | A | 1 | a0001c0001t0004g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-32-10731G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814277 | |||||||
| chr4:184814286 | G | A | 11 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(8): Show |
11 | HG01081.hp2 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-10740C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814286 | |||||||
| chr4:184814290 | C | CA | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
212 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-32-10745dupT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814290 | |||||||
| chr4:184814290 | C | CAA | 21 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0127 others(18): Show |
22 | HG00738.hp1 HG01167.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32-10746_-32-1074 others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814290 | |||||||
| chr4:184814290 | CA | C | 12 | a0001c0001t0001g0182 a0001c0001t0001g0198 a0001c0001t0002g0148 others(9): Show |
12 | HG01069.hp1 HG01081.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-10745delT | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814290 | |||||||
| chr4:184814290 | CAAA | C | 8 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0345 others(5): Show |
8 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-10747_-32-1074 others(7): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814290 | |||||||
| chr4:184814339 | C | T | 2 | a0001c0002t0002g0105 a0001c0004t0001g0104 |
2 | HG01928.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-32-10793G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814339 | |||||||
| chr4:184814400 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-32-10854C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814400 | |||||||
| chr4:184814400 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-32-10854C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814400 | |||||||
| chr4:184814420 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-32-10874C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814420 | |||||||
| chr4:184814524 | G | A | 9 | a0001c0001t0004g0138 a0001c0001t0004g0143 a0001c0001t0004g0144 others(6): Show |
9 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-10978C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814524 | |||||||
| chr4:184814533 | G | C | 3 | a0001c0001t0001g0171 a0001c0001t0002g0013 a0001c0001t0002g0170 |
4 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-10987C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814533 | |||||||
| chr4:184814547 | T | C | 10 | a0001c0001t0004g0337 a0001c0001t0004g0338 a0001c0001t0004g0351 others(7): Show |
10 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-11001A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814547 | |||||||
| chr4:184814837 | G | A | 2 | a0001c0001t0001g0102 a0001c0002t0002g0103 |
2 | HG02135.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-33+11079C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814837 | |||||||
| chr4:184814959 | G | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(168): Show |
181 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.-33+10957C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184814959 | |||||||
| chr4:184815001 | G | A | 1 | a0001c0005t0003g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+10915C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815001 | |||||||
| chr4:184815005 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-33+10911A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815005 | |||||||
| chr4:184815076 | G | C | 1 | a0001c0002t0002g0179 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-33+10840C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815076 | |||||||
| chr4:184815160 | T | G | 17 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(14): Show |
18 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33+10756A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815160 | |||||||
| chr4:184815163 | G | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-33+10753C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815163 | |||||||
| chr4:184815255 | G | A | 1 | a0001c0003t0003g0012 | 2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-33+10661C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815255 | |||||||
| chr4:184815299 | C | T | 15 | a0001c0001t0004g0138 a0001c0001t0004g0143 a0001c0001t0004g0144 others(12): Show |
15 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+10617G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815299 | |||||||
| chr4:184815337 | C | T | 1 | a0001c0002t0002g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-33+10579G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815337 | |||||||
| chr4:184815489 | T | TG | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0148 others(31): Show |
34 | HG00639.hp1 HG01069.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+10426dupC | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815489 | |||||||
| chr4:184815495 | G | C | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+10421C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815495 | |||||||
| chr4:184815535 | G | A | 9 | a0001c0001t0002g0364 a0001c0001t0002g0365 a0001c0001t0002g0366 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33+10381C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815535 | |||||||
| chr4:184815547 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-33+10369G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184815547 | |||||||
| chr4:184816050 | G | A | 1 | a0001c0001t0002g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-33+9866C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816050 | |||||||
| chr4:184816053 | C | T | 9 | a0001c0001t0004g0138 a0001c0001t0004g0143 a0001c0001t0004g0144 others(6): Show |
9 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33+9863G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816053 | |||||||
| chr4:184816059 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-33+9857C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816059 | |||||||
| chr4:184816208 | A | C | 1 | a0001c0002t0002g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-33+9708T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816208 | |||||||
| chr4:184816247 | T | C | 2 | a0001c0002t0002g0216 a0001c0002t0002g0217 |
2 | NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-33+9669A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816247 | |||||||
| chr4:184816471 | T | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(20): Show |
25 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-33+9445A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816471 | |||||||
| chr4:184816516 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-33+9400C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816516 | |||||||
| chr4:184816684 | T | C | 1 | a0001c0001t0004g0357 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-33+9232A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816684 | |||||||
| chr4:184816689 | G | A | 80 | a0001c0001t0001g0015 a0001c0001t0001g0169 a0001c0001t0001g0171 others(77): Show |
83 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.-33+9227C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816689 | |||||||
| chr4:184816711 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-33+9205T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816711 | |||||||
| chr4:184816800 | C | T | 21 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0172 others(18): Show |
22 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-33+9116G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816800 | |||||||
| chr4:184816820 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-33+9096C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816820 | |||||||
| chr4:184816975 | T | C | 1 | a0001c0001t0010g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-33+8941A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184816975 | |||||||
| chr4:184817007 | G | C | 1 | a0001c0001t0004g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-33+8909C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817007 | |||||||
| chr4:184817092 | A | T | 5 | a0001c0001t0002g0148 a0001c0001t0002g0231 a0001c0005t0012g0149 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+8824T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817092 | |||||||
| chr4:184817122 | T | A | 1 | a0001c0001t0004g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-33+8794A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817122 | |||||||
| chr4:184817269 | G | T | 1 | a0001c0003t0003g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-33+8647C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817269 | |||||||
| chr4:184817406 | A | G | 2 | a0001c0001t0001g0235 a0001c0003t0003g0349 |
2 | HG01255.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-33+8510T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817406 | |||||||
| chr4:184817456 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0010g0157 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-33+8460C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817456 | |||||||
| chr4:184817468 | C | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-33+8448G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817468 | |||||||
| chr4:184817581 | G | A | 5 | a0001c0001t0002g0148 a0001c0001t0002g0231 a0001c0005t0012g0149 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+8335C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817581 | |||||||
| chr4:184817625 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-33+8291C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817625 | |||||||
| chr4:184817625 | G | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-33+8291C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817625 | |||||||
| chr4:184817650 | C | G | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(7): Show |
11 | HG01081.hp2 HG01167.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33+8266G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817650 | |||||||
| chr4:184817756 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-33+8160C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817756 | |||||||
| chr4:184817768 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-33+8148G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817768 | |||||||
| chr4:184817772 | G | A | 1 | a0001c0003t0003g0340 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-33+8144C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184817772 | |||||||
| chr4:184818092 | C | T | 5 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0002g0013 others(2): Show |
6 | HG00733.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+7824G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818092 | |||||||
| chr4:184818099 | G | C | 1 | a0001c0002t0002g0179 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-33+7817C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818099 | |||||||
| chr4:184818556 | C | T | 2 | a0001c0001t0001g0234 a0001c0003t0003g0233 |
2 | NA19002.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-33+7360G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818556 | |||||||
| chr4:184818663 | C | T | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-33+7253G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818663 | |||||||
| chr4:184818740 | G | C | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(4): Show |
8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+7176C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818740 | |||||||
| chr4:184818814 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-33+7102G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818814 | |||||||
| chr4:184818910 | T | C | 23 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(20): Show |
24 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-33+7006A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818910 | |||||||
| chr4:184818912 | T | A | 1 | a0001c0002t0002g0156 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+7004A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184818912 | |||||||
| chr4:184819060 | G | A | 1 | a0001c0001t0002g0348 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-33+6856C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819060 | |||||||
| chr4:184819061 | C | T | 19 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(16): Show |
20 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-33+6855G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819061 | |||||||
| chr4:184819140 | C | CT | 12 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0198 others(9): Show |
12 | HG00099.hp1 HG01099.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33+6775dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819140 | |||||||
| chr4:184819140 | CT | C | 44 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0169 others(41): Show |
46 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.-33+6775delA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819140 | |||||||
| chr4:184819140 | CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0002g0148 a0001c0001t0002g0158 a0001c0001t0002g0363 others(7): Show |
10 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33+6766_-33+6775d others(12): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819140 | |||||||
| chr4:184819142 | T | C | 21 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0172 others(18): Show |
22 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-33+6774A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819142 | |||||||
| chr4:184819169 | G | T | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(4): Show |
8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+6747C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819169 | |||||||
| chr4:184819211 | T | C | 30 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(27): Show |
32 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-33+6705A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819211 | |||||||
| chr4:184819535 | C | T | 1 | a0001c0006t0002g0037 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-33+6381G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819535 | |||||||
| chr4:184819602 | TAC | T | 7 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+6312_-33+6313d others(4): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819602 | |||||||
| chr4:184819618 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33+6298G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819618 | |||||||
| chr4:184819969 | G | C | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(4): Show |
8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5947C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184819969 | |||||||
| chr4:184820035 | A | AACAGGC | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(4): Show |
8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5875_-33+5880d others(8): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820035 | |||||||
| chr4:184820121 | C | T | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(4): Show |
8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5795G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820121 | |||||||
| chr4:184820212 | T | G | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+5704A>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820212 | |||||||
| chr4:184820306 | T | C | 1 | a0001c0002t0002g0342 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-33+5610A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820306 | |||||||
| chr4:184820324 | C | T | 2 | a0001c0001t0002g0158 a0001c0001t0010g0157 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-33+5592G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820324 | |||||||
| chr4:184820327 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-33+5589G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820327 | |||||||
| chr4:184820443 | C | A | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(4): Show |
8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5473G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820443 | |||||||
| chr4:184820607 | C | CT | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0222 others(4): Show |
8 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+5308dupA | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820607 | |||||||
| chr4:184820609 | T | C | 6 | a0001c0001t0002g0363 a0001c0001t0002g0364 a0001c0001t0002g0365 others(3): Show |
6 | HG01516.hp2 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+5307A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820609 | |||||||
| chr4:184820642 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-33+5274A>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820642 | |||||||
| chr4:184820665 | C | T | 1 | a0001c0002t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-33+5251G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820665 | |||||||
| chr4:184820704 | A | T | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-33+5212T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820704 | |||||||
| chr4:184820708 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0136 a0001c0001t0001g0137 others(5): Show |
10 | HG01891.hp2 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33+5208C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820708 | |||||||
| chr4:184820793 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-33+5123G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820793 | |||||||
| chr4:184820860 | C | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(9): Show |
14 | HG01074.hp1 HG01109.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+5056G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184820860 | |||||||
| chr4:184821255 | C | T | 2 | a0001c0001t0002g0196 a0001c0002t0002g0156 |
2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-33+4661G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184821255 | |||||||
| chr4:184821305 | G | C | 3 | a0001c0005t0012g0149 a0001c0005t0014g0151 a0003c0012t0002g0150 |
3 | HG02258.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-33+4611C>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184821305 | |||||||
| chr4:184821422 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(5): Show |
10 | HG01074.hp1 HG01109.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33+4494G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184821422 | |||||||
| chr4:184821956 | C | T | 1 | a0001c0001t0004g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-33+3960G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184821956 | |||||||
| chr4:184822194 | C | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(201): Show |
221 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.-33+3722G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822194 | |||||||
| chr4:184822537 | G | A | 1 | a0001c0002t0002g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-33+3379C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822537 | |||||||
| chr4:184822564 | G | A | 1 | a0001c0003t0003g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-33+3352C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822564 | |||||||
| chr4:184822584 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(202): Show |
222 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(219): Show |
intron_variant | MODIFIER | c.-33+3332G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822584 | |||||||
| chr4:184822672 | G | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0002g0007 others(3): Show |
7 | HG02074.hp2 NA18941.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+3244C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822672 | |||||||
| chr4:184822834 | T | C | 17 | a0001c0001t0001g0015 a0001c0001t0001g0182 a0001c0001t0001g0183 others(14): Show |
19 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-33+3082A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822834 | |||||||
| chr4:184822860 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-33+3056T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822860 | |||||||
| chr4:184822916 | C | A | 1 | a0001c0002t0002g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-33+3000G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822916 | |||||||
| chr4:184822949 | T | C | 3 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 |
3 | HG01081.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-33+2967A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184822949 | |||||||
| chr4:184823177 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-33+2739G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823177 | |||||||
| chr4:184823270 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-33+2646T>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823270 | |||||||
| chr4:184823508 | T | C | 1 | a0001c0005t0003g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-33+2408A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823508 | |||||||
| chr4:184823649 | A | T | 1 | a0001c0003t0003g0029 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-33+2267T>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823649 | |||||||
| chr4:184823666 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(118): Show |
134 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.-33+2250G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823666 | |||||||
| chr4:184823741 | A | C | 1 | a0001c0001t0001g0028 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-33+2175T>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823741 | |||||||
| chr4:184823768 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+2148A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823768 | |||||||
| chr4:184823875 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(201): Show |
221 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.-33+2041G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184823875 | |||||||
| chr4:184824257 | C | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0002t0002g0005 others(3): Show |
8 | NA18965.hp2 NA18967.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+1659G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824257 | |||||||
| chr4:184824283 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+1633C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824283 | |||||||
| chr4:184824286 | TG | T | 10 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0004g0143 others(7): Show |
10 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33+1629delC | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824286 | |||||||
| chr4:184824416 | G | A | 1 | a0001c0002t0002g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-33+1500C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824416 | |||||||
| chr4:184824456 | T | C | 54 | a0001c0001t0001g0015 a0001c0001t0001g0166 a0001c0001t0001g0169 others(51): Show |
58 | HG00733.hp2 HG01074.hp1 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-33+1460A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824456 | |||||||
| chr4:184824486 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(201): Show |
221 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.-33+1430A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824486 | |||||||
| chr4:184824835 | AAAAG | A | 5 | a0001c0001t0002g0363 a0001c0001t0002g0364 a0001c0001t0002g0365 others(2): Show |
5 | HG02647.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+1077_-33+1080d others(6): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824835 | |||||||
| chr4:184824934 | G | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(203): Show |
223 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.-33+982C>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184824934 | |||||||
| chr4:184825019 | G | A | 9 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(6): Show |
10 | HG01167.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33+897C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825019 | |||||||
| chr4:184825103 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(131): Show |
142 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-33+813A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825103 | |||||||
| chr4:184825147 | C | A | 1 | a0001c0003t0003g0349 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33+769G>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825147 | |||||||
| chr4:184825173 | G | A | 1 | a0001c0001t0001g0350 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-33+743C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825173 | |||||||
| chr4:184825341 | T | C | 7 | a0001c0001t0004g0351 a0001c0001t0004g0352 a0001c0001t0004g0353 others(4): Show |
7 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+575A>G | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825341 | |||||||
| chr4:184825411 | C | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(120): Show |
136 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.-33+505G>C | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825411 | |||||||
| chr4:184825673 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
142 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.-33+243G>A | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825673 | |||||||
| chr4:184825735 | G | A | 4 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(1): Show |
4 | HG00597.hp2 HG02165.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+181C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825735 | |||||||
| chr4:184825788 | G | A | 5 | a0001c0001t0002g0363 a0001c0001t0002g0364 a0001c0001t0002g0365 others(2): Show |
5 | HG02647.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+128C>T | ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | 184825788 |