Item | Value |
---|---|
geneid | 10965 |
ensemblid | ENSG00000119673.16 |
hgncid | 18431 |
symbol | ACOT2 |
name | acyl-CoA thioesterase 2 |
refseq_nuc | NM_006821.6 |
refseq_prot | NP_006812.3 |
ensembl_nuc | ENST00000238651.10 |
ensembl_prot | ENSP00000238651.5 |
mane_status | MANE Select |
chr | chr14 |
start | 73569213 |
end | 73575655 |
strand | + |
ver | v1.2 |
region | chr14:73569213-73575655 |
region5000 | chr14:73564213-73580655 |
regionname0 | ACOT2_chr14_73569213_73575655 |
regionname5000 | ACOT2_chr14_73564213_73580655 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1449 | 423 | 92 | 77 | 194 | 14 | 44 | ACOT2_chr14_73564213_73580655 | ACOT2 | ATGTC others(1444): Show |
chr14 | 73564213 | 73580655 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1622 | 423 | 92 | 77 | 194 | 14 | 44 | ACOT2_chr14_73564213_73580655 | ACOT2 | GCTTA others(1617): Show |
chr14 | 73564213 | 73580655 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 422 | 92 | 77 | 194 | 14 | 44 | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
a0001c0001t0001g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0002 | REF | REF | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | ACOT2_chr14_73564213_73580655 | ACOT2 | chr14 | 73564213 | 73580655 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73569256 | C | T | 1 | a0001 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.16C>T | p.Leu6Phe | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 44/1622 | 16/1452 | 6/483 | chr14 | 73569256 | |||
chr14:73569512 | A | G | 1 | a0001 | 9 | HG01361.hp1 HG02135.hp2 HG02165.hp2 others(6): Show |
missense_variant | MODERATE | c.272A>G | p.Glu91Gly | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 300/1622 | 272/1452 | 91/483 | chr14 | 73569512 | |||
chr14:73569551 | A | G | 1 | a0001 | 6 | HG01243.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
missense_variant | MODERATE | c.311A>G | p.Lys104Arg | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 339/1622 | 311/1452 | 104/483 | chr14 | 73569551 | |||
chr14:73569557 | C | A | 1 | a0001 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.317C>A | p.Ala106Glu | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 345/1622 | 317/1452 | 106/483 | chr14 | 73569557 | |||
chr14:73569667 | C | T | 1 | a0001 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.427C>T | p.Leu143Phe | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 455/1622 | 427/1452 | 143/483 | chr14 | 73569667 | |||
chr14:73569773 | C | G | 1 | a0001 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.533C>G | p.Pro178Arg | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 561/1622 | 533/1452 | 178/483 | chr14 | 73569773 | |||
chr14:73569791 | A | G | 1 | a0001 | 2 | HG01106.hp2 HG04228.hp1 |
missense_variant | MODERATE | c.551A>G | p.Gln184Arg | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 579/1622 | 551/1452 | 184/483 | chr14 | 73569791 | |||
chr14:73569793 | A | G | 1 | a0001 | 2 | HG01106.hp2 HG04228.hp1 |
missense_variant | MODERATE | c.553A>G | p.Thr185Ala | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 581/1622 | 553/1452 | 185/483 | chr14 | 73569793 | |||
chr14:73569794 | C | T | 1 | a0001 | 2 | HG01106.hp2 HG04228.hp1 |
missense_variant | MODERATE | c.554C>T | p.Thr185Met | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 582/1622 | 554/1452 | 185/483 | chr14 | 73569794 | |||
chr14:73573408 | A | T | 1 | a0001 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.664A>T | p.Ile222Phe | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/3 | 692/1622 | 664/1452 | 222/483 | chr14 | 73573408 | |||
chr14:73573432 | G | A | 1 | a0001 | 4 | HG01433.hp1 HG02129.hp2 HG02602.hp1 others(1): Show |
missense_variant | MODERATE | c.688G>A | p.Gly230Ser | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/3 | 716/1622 | 688/1452 | 230/483 | chr14 | 73573432 | |||
chr14:73573517 | T | A | 1 | a0001 | 3 | NA18940.hp1 NA19007.hp2 NA19079.hp1 |
missense_variant | MODERATE | c.773T>A | p.Leu258His | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/3 | 801/1622 | 773/1452 | 258/483 | chr14 | 73573517 | |||
chr14:73574921 | G | A | 1 | a0001 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.860G>A | p.Gly287Glu | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 888/1622 | 860/1452 | 287/483 | chr14 | 73574921 | |||
chr14:73574981 | T | C | 1 | a0001 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.920T>C | p.Leu307Pro | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 948/1622 | 920/1452 | 307/483 | chr14 | 73574981 | |||
chr14:73575044 | A | G | 1 | a0001 | 371 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(368): Show |
missense_variant | MODERATE | c.983A>G | p.His328Arg | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 1011/1622 | 983/1452 | 328/483 | chr14 | 73575044 | |||
chr14:73575071 | T | C | 1 | a0001 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.1010T>C | p.Val337Ala | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 1038/1622 | 1010/1452 | 337/483 | chr14 | 73575071 | |||
chr14:73575074 | G | C | 1 | a0001 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.1013G>C | p.Gly338Ala | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 1041/1622 | 1013/1452 | 338/483 | chr14 | 73575074 | |||
chr14:73575391 | A | G | 1 | a0001 | 6 | HG01109.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
missense_variant | MODERATE | c.1330A>G | p.Ile444Val | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 1358/1622 | 1330/1452 | 444/483 | chr14 | 73575391 | |||
chr14:73575485 | A | G | 1 | a0001 | 268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
missense_variant | MODERATE | c.1424A>G | p.His475Arg | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 1452/1622 | 1424/1452 | 475/483 | chr14 | 73575485 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73569594 | T | C | 1 | a0001c0001 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.354T>C | p.Thr118Thr | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 382/1622 | 354/1452 | 118/483 | chr14 | 73569594 | |||
chr14:73569666 | G | T | 1 | a0001c0001 | 23 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(20): Show |
synonymous_variant | LOW | c.426G>T | p.Leu142Leu | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/3 | 454/1622 | 426/1452 | 142/483 | chr14 | 73569666 | |||
chr14:73575477 | G | A | 1 | a0001c0001 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1416G>A | p.Leu472Leu | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 1444/1622 | 1416/1452 | 472/483 | chr14 | 73575477 | |||
chr14:73575486 | C | T | 1 | a0001c0001 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1425C>T | p.His475His | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 1453/1622 | 1425/1452 | 475/483 | chr14 | 73575486 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73575520 | T | A | 1 | a0001c0001t0001 | 7 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7T>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 7 | chr14 | 73575520 | ||||||
chr14:73575613 | C | T | 1 | a0001c0001t0001 | 16 | HG00140.hp2 HG00738.hp1 HG01069.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*100C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 3/3 | 100 | chr14 | 73575613 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73569909 | G | T | 1 | a0001c0001t0001g0001 | 15 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.643+26G>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73569909 | |||||||
chr14:73569970 | G | GC | 1 | a0001c0001t0001g0001 | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.643+94dupC | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73569970 | ||||||
chr14:73569976 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.643+93C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73569976 | |||||||
chr14:73570060 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.643+177C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570060 | |||||||
chr14:73570110 | C | CT | 1 | a0001c0001t0001g0001 | 226 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.643+240dupT | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73570110 | ||||||
chr14:73570123 | T | TC | 1 | a0001c0001t0001g0001 | 15 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.643+242dupC | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73570123 | ||||||
chr14:73570289 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.643+406G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570289 | |||||||
chr14:73570328 | G | C | 1 | a0001c0001t0001g0001 | 4 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.643+445G>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570328 | |||||||
chr14:73570383 | C | G | 1 | a0001c0001t0001g0001 | 8 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.643+500C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570383 | |||||||
chr14:73570486 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.643+603G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570486 | |||||||
chr14:73570642 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.643+759C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570642 | |||||||
chr14:73570644 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.643+761C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570644 | |||||||
chr14:73570679 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.643+796C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570679 | |||||||
chr14:73570736 | C | G | 1 | a0001c0001t0001g0001 | 23 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.643+853C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570736 | |||||||
chr14:73570747 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.643+864A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570747 | |||||||
chr14:73570876 | GCCTGGGG others(32): Show |
G | 1 | a0001c0001t0001g0001 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.643+994_643+1032de others(40): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570876 | |||||||
chr14:73570894 | A | T | 1 | a0001c0001t0001g0001 | 6 | HG01243.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.643+1011A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570894 | |||||||
chr14:73570903 | TA | T | 1 | a0001c0001t0001g0001 | 146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.643+1038delA | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73570903 | ||||||
chr14:73570903 | TAA | T | 1 | a0001c0001t0001g0001 | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.643+1037_643+1038d others(4): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73570903 | ||||||
chr14:73570903 | TAAA | T | 1 | a0001c0001t0001g0001 | 8 | HG01515.hp1 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.643+1036_643+1038d others(5): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73570903 | ||||||
chr14:73570975 | AC | A | 1 | a0001c0001t0001g0001 | 119 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.643+1093delC | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570975 | |||||||
chr14:73570976 | C | CT | 1 | a0001c0001t0001g0001 | 87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.643+1107dupT | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73570976 | ||||||
chr14:73570976 | C | CTT | 1 | a0001c0001t0001g0001 | 8 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.643+1106_643+1107d others(4): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73570976 | ||||||
chr14:73570976 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.643+1093C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570976 | |||||||
chr14:73570990 | TA | T | 1 | a0001c0001t0001g0001 | 19 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.643+1110delA | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73570990 | ||||||
chr14:73570991 | A | T | 1 | a0001c0001t0001g0001 | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.643+1108A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73570991 | |||||||
chr14:73571026 | C | T | 1 | a0001c0001t0001g0001 | 85 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.643+1143C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571026 | |||||||
chr14:73571144 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG00621.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.643+1261T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571144 | |||||||
chr14:73571159 | C | T | 1 | a0001c0001t0001g0001 | 73 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.643+1276C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571159 | |||||||
chr14:73571160 | G | C | 1 | a0001c0001t0001g0001 | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.643+1277G>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571160 | |||||||
chr14:73571168 | G | A | 1 | a0001c0001t0001g0001 | 8 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.643+1285G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571168 | |||||||
chr14:73571179 | CCT | C | 1 | a0001c0001t0001g0001 | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.643+1297_643+1298d others(4): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571179 | |||||||
chr14:73571259 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.643+1376G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571259 | |||||||
chr14:73571367 | G | A | 1 | a0001c0001t0001g0001 | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.643+1484G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571367 | |||||||
chr14:73571465 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.643+1582C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571465 | |||||||
chr14:73571499 | G | C | 1 | a0001c0001t0001g0001 | 6 | HG01243.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.643+1616G>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571499 | |||||||
chr14:73571507 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.643+1624C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571507 | |||||||
chr14:73571510 | G | A | 1 | a0001c0001t0001g0001 | 391 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(388): Show |
intron_variant | MODIFIER | c.643+1627G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571510 | |||||||
chr14:73571575 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.643+1692G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571575 | |||||||
chr14:73571583 | T | C | 1 | a0001c0001t0001g0001 | 23 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.643+1700T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571583 | |||||||
chr14:73571612 | G | C | 1 | a0001c0001t0001g0001 | 24 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.643+1729G>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571612 | |||||||
chr14:73571628 | G | A | 1 | a0001c0001t0001g0001 | 23 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.643+1745G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571628 | |||||||
chr14:73571634 | G | T | 1 | a0001c0001t0001g0001 | 23 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.643+1751G>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571634 | |||||||
chr14:73571656 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01074.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.644-1732C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571656 | |||||||
chr14:73571679 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.644-1709C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571679 | |||||||
chr14:73571680 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.644-1708G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571680 | |||||||
chr14:73571703 | C | T | 1 | a0001c0001t0001g0001 | 10 | HG01361.hp1 HG02135.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.644-1685C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571703 | |||||||
chr14:73571707 | G | A | 1 | a0001c0001t0001g0001 | 4 | HG00733.hp1 HG00735.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.644-1681G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571707 | |||||||
chr14:73571721 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.644-1667C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571721 | |||||||
chr14:73571845 | T | G | 1 | a0001c0001t0001g0001 | 6 | HG00423.hp2 HG00438.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.644-1543T>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73571845 | |||||||
chr14:73572059 | TGCTA | T | 1 | a0001c0001t0001g0001 | 5 | HG02258.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.644-1327_644-1324d others(6): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572059 | ||||||
chr14:73572113 | C | T | 1 | a0001c0001t0001g0001 | 45 | HG00140.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.644-1275C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572113 | |||||||
chr14:73572118 | T | G | 1 | a0001c0001t0001g0001 | 45 | HG00140.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.644-1270T>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572118 | |||||||
chr14:73572174 | G | GAAAGCCA others(2): Show |
1 | a0001c0001t0001g0001 | 389 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(386): Show |
intron_variant | MODIFIER | c.644-1214_644-1213i others(11): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572174 | |||||||
chr14:73572175 | C | G | 1 | a0001c0001t0001g0001 | 389 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(386): Show |
intron_variant | MODIFIER | c.644-1213C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572175 | |||||||
chr14:73572214 | G | T | 1 | a0001c0001t0001g0001 | 7 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.644-1174G>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572214 | |||||||
chr14:73572308 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.644-1080C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572308 | |||||||
chr14:73572358 | C | G | 1 | a0001c0001t0001g0001 | 185 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.644-1030C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572358 | |||||||
chr14:73572381 | A | T | 1 | a0001c0001t0001g0001 | 15 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.644-1007A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572381 | |||||||
chr14:73572404 | C | A | 1 | a0001c0001t0001g0001 | 9 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.644-984C>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572404 | |||||||
chr14:73572412 | A | AAC | 1 | a0001c0001t0001g0001 | 15 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.644-972_644-971dup others(2): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572412 | ||||||
chr14:73572443 | A | G | 1 | a0001c0001t0001g0001 | 203 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.644-945A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572443 | |||||||
chr14:73572452 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.644-936C>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572452 | |||||||
chr14:73572587 | C | T | 1 | a0001c0001t0001g0001 | 8 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.644-801C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572587 | |||||||
chr14:73572600 | T | C | 1 | a0001c0001t0001g0001 | 22 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.644-788T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572600 | |||||||
chr14:73572626 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.644-762G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572626 | |||||||
chr14:73572639 | ATT | A | 1 | a0001c0001t0001g0001 | 12 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.644-724_644-723del others(2): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572639 | ||||||
chr14:73572639 | ATTT | A | 1 | a0001c0001t0001g0001 | 88 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.644-725_644-723del others(3): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572639 | ||||||
chr14:73572639 | ATTTT | A | 1 | a0001c0001t0001g0001 | 22 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.644-726_644-723del others(4): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572639 | ||||||
chr14:73572639 | ATTTTT | A | 1 | a0001c0001t0001g0001 | 15 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.644-727_644-723del others(5): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572639 | ||||||
chr14:73572639 | ATTTTTTT others(1): Show |
A | 1 | a0001c0001t0001g0001 | 13 | HG00673.hp1 HG01361.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.644-730_644-723del others(8): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572639 | ||||||
chr14:73572639 | ATTTTTTT others(2): Show |
A | 1 | a0001c0001t0001g0001 | 228 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.644-731_644-723del others(9): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572639 | ||||||
chr14:73572639 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0001 | 8 | HG01884.hp2 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.644-732_644-723del others(10): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572639 | ||||||
chr14:73572639 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0001 | 5 | HG02258.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.644-733_644-723del others(11): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73572639 | ||||||
chr14:73572644 | T | C | 1 | a0001c0001t0001g0001 | 12 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.644-744T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572644 | |||||||
chr14:73572645 | T | C | 1 | a0001c0001t0001g0001 | 88 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.644-743T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572645 | |||||||
chr14:73572646 | T | C | 1 | a0001c0001t0001g0001 | 22 | HG01123.hp2 HG01255.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.644-742T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572646 | |||||||
chr14:73572647 | T | C | 1 | a0001c0001t0001g0001 | 15 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.644-741T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572647 | |||||||
chr14:73572650 | T | C | 1 | a0001c0001t0001g0001 | 13 | HG00673.hp1 HG01361.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.644-738T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572650 | |||||||
chr14:73572651 | T | C | 1 | a0001c0001t0001g0001 | 228 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.644-737T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572651 | |||||||
chr14:73572652 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA19043.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.644-736T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572652 | |||||||
chr14:73572679 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.644-709G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572679 | |||||||
chr14:73572720 | A | T | 1 | a0001c0001t0001g0001 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.644-668A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572720 | |||||||
chr14:73572733 | C | A | 1 | a0001c0001t0001g0001 | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.644-655C>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572733 | |||||||
chr14:73572738 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02738.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.644-650C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572738 | |||||||
chr14:73572787 | A | G | 1 | a0001c0001t0001g0001 | 5 | HG02258.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.644-601A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572787 | |||||||
chr14:73572833 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.644-555A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572833 | |||||||
chr14:73572912 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.644-476C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572912 | |||||||
chr14:73572917 | G | A | 1 | a0001c0001t0001g0001 | 420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.644-471G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572917 | |||||||
chr14:73572930 | G | C | 1 | a0001c0001t0001g0001 | 35 | HG00140.hp2 HG00738.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.644-458G>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572930 | |||||||
chr14:73572936 | G | A | 1 | a0001c0001t0001g0001 | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.644-452G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572936 | |||||||
chr14:73572949 | A | C | 1 | a0001c0001t0001g0001 | 15 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.644-439A>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572949 | |||||||
chr14:73572956 | C | T | 1 | a0001c0001t0001g0001 | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.644-432C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572956 | |||||||
chr14:73572958 | A | C | 1 | a0001c0001t0001g0001 | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.644-430A>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73572958 | |||||||
chr14:73573006 | A | AT | 1 | a0001c0001t0001g0001 | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.644-381dupT | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73573006 | ||||||
chr14:73573055 | G | A | 1 | a0001c0001t0001g0001 | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.644-333G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73573055 | |||||||
chr14:73573060 | G | A | 1 | a0001c0001t0001g0001 | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.644-328G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73573060 | |||||||
chr14:73573385 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02165.hp2 | splice_region_variant&intron_variant | LOW | c.644-3A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 1/2 | chr14 | 73573385 | |||||||
chr14:73573637 | T | C | 1 | a0001c0001t0001g0001 | 123 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.846+47T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573637 | |||||||
chr14:73573648 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.846+58C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573648 | |||||||
chr14:73573679 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+89A>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573679 | |||||||
chr14:73573680 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+90C>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573680 | |||||||
chr14:73573687 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+97T>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573687 | |||||||
chr14:73573690 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+100C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573690 | |||||||
chr14:73573698 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+108A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573698 | |||||||
chr14:73573699 | C | G | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+109C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573699 | |||||||
chr14:73573710 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.846+120T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573710 | |||||||
chr14:73573721 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+131C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573721 | |||||||
chr14:73573734 | G | GTTTCTTT others(17): Show |
1 | a0001c0001t0001g0001 | 13 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.846+151_846+152ins others(24): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73573734 | ||||||
chr14:73573746 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+156G>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573746 | |||||||
chr14:73573747 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+157A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573747 | |||||||
chr14:73573749 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+159A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573749 | |||||||
chr14:73573753 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+163A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573753 | |||||||
chr14:73573754 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+164G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573754 | |||||||
chr14:73573756 | C | G | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+166C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573756 | |||||||
chr14:73573757 | T | C | 1 | a0001c0001t0001g0001 | 16 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.846+167T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573757 | |||||||
chr14:73573758 | C | G | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+168C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573758 | |||||||
chr14:73573759 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+169A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573759 | |||||||
chr14:73573761 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+171T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573761 | |||||||
chr14:73573766 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.846+176T>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573766 | |||||||
chr14:73573808 | C | A | 1 | a0001c0001t0001g0001 | 6 | HG01243.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+218C>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573808 | |||||||
chr14:73573846 | C | G | 1 | a0001c0001t0001g0001 | 3 | HG02135.hp2 NA18994.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.846+256C>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573846 | |||||||
chr14:73573858 | T | C | 1 | a0001c0001t0001g0001 | 391 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(388): Show |
intron_variant | MODIFIER | c.846+268T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573858 | |||||||
chr14:73573942 | G | T | 1 | a0001c0001t0001g0001 | 17 | HG01361.hp1 HG02109.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.846+352G>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573942 | |||||||
chr14:73573965 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.846+375G>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73573965 | |||||||
chr14:73574030 | A | T | 1 | a0001c0001t0001g0001 | 5 | HG02258.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.846+440A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574030 | |||||||
chr14:73574036 | AT | A | 1 | a0001c0001t0001g0001 | 391 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(388): Show |
intron_variant | MODIFIER | c.846+459delT | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73574036 | ||||||
chr14:73574060 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.846+470G>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574060 | |||||||
chr14:73574067 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.846+477C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574067 | |||||||
chr14:73574115 | C | T | 1 | a0001c0001t0001g0001 | 6 | HG02698.hp1 HG03491.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+525C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574115 | |||||||
chr14:73574139 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.846+549G>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574139 | |||||||
chr14:73574172 | CTT | C | 1 | a0001c0001t0001g0001 | 3 | HG02723.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.846+583_846+584del others(2): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574172 | |||||||
chr14:73574235 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.846+645T>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574235 | |||||||
chr14:73574263 | A | AT | 1 | a0001c0001t0001g0001 | 8 | HG02258.hp2 HG03098.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.847-626dupT | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73574263 | ||||||
chr14:73574263 | A | T | 1 | a0001c0001t0001g0001 | 2 | HG01074.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.847-645A>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574263 | |||||||
chr14:73574263 | AT | A | 1 | a0001c0001t0001g0001 | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.847-626delT | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73574263 | ||||||
chr14:73574263 | ATT | A | 1 | a0001c0001t0001g0001 | 34 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.847-627_847-626del others(2): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73574263 | ||||||
chr14:73574352 | C | A | 1 | a0001c0001t0001g0001 | 115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.847-556C>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574352 | |||||||
chr14:73574391 | C | A | 1 | a0001c0001t0001g0001 | 27 | HG01243.hp1 HG01361.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.847-517C>A | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574391 | |||||||
chr14:73574391 | C | T | 1 | a0001c0001t0001g0001 | 3 | NA18959.hp1 NA19054.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.847-517C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574391 | |||||||
chr14:73574410 | A | G | 1 | a0001c0001t0001g0001 | 49 | HG00140.hp2 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.847-498A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574410 | |||||||
chr14:73574414 | G | C | 1 | a0001c0001t0001g0001 | 27 | HG01243.hp1 HG01361.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.847-494G>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574414 | |||||||
chr14:73574543 | G | GTCAGCCA others(30): Show |
1 | a0001c0001t0001g0001 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.847-349_847-348ins others(37): Show |
ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73574543 | ||||||
chr14:73574765 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.847-143A>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574765 | |||||||
chr14:73574771 | T | C | 1 | a0001c0001t0001g0001 | 30 | HG01243.hp1 HG01361.hp1 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.847-137T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574771 | |||||||
chr14:73574777 | T | C | 1 | a0001c0001t0001g0001 | 11 | HG01496.hp1 HG01884.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.847-131T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574777 | |||||||
chr14:73574804 | T | C | 1 | a0001c0001t0001g0001 | 4 | HG01975.hp1 HG02148.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-104T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574804 | |||||||
chr14:73574822 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.847-86C>T | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574822 | |||||||
chr14:73574841 | A | G | 1 | a0001c0001t0001g0001 | 3 | HG01975.hp1 HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.847-67A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574841 | |||||||
chr14:73574872 | A | G | 1 | a0001c0001t0001g0001 | 3 | HG01975.hp1 HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.847-36A>G | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574872 | |||||||
chr14:73574873 | T | C | 1 | a0001c0001t0001g0001 | 3 | HG01975.hp1 HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.847-35T>C | ACOT2 | ENSG00000119673.16 | transcript | ENST00000238651.10 | protein_coding | 2/2 | chr14 | 73574873 |