Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5465 |
|---|---|
| ensemblid | ENSG00000186951.17 |
| hgncid | 9232 |
| symbol | PPARA |
| name | peroxisome proliferator activated receptor alpha |
| refseq_nuc | NM_005036.6 |
| refseq_prot | NP_005027.2 |
| ensembl_nuc | ENST00000407236.6 |
| ensembl_prot | ENSP00000385523.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 46150526 |
| end | 46243755 |
| strand | + |
| ver | v1.2 |
| region | chr22:46150526-46243755 |
| region5000 | chr22:46145526-46248755 |
| regionname0 | PPARA_chr22_46150526_46243755 |
| regionname5000 | PPARA_chr22_46145526_46248755 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 468 | 189 | 90 | 35 | 36 | 5 | 21 | 20 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0002 | 0/0 | 468 | 6 | 0 | 3 | 3 | 0 | 0 | 3 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0003 | 0/0 | 468 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0004 | 0/0 | 468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1407 | 182 | 88 | 32 | 34 | 5 | 21 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| c0002 | 0/0 | 1407 | 6 | 0 | 3 | 3 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| c0003 | 0/0 | 1407 | 4 | 0 | 2 | 0 | 1 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| c0004 | 0/0 | 1407 | 2 | 0 | 0 | 2 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| c0005 | 0/0 | 1407 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| c0006 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| c0007 | 0/0 | 1407 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| c0008 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 8712 | 34 | 3 | 9 | 13 | 3 | 5 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0002 | 0/0 | 8714 | 21 | 8 | 2 | 9 | 0 | 2 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0003 | 0/0 | 8709 | 8 | 8 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0004 | 0/0 | 8717 | 8 | 7 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0005 | 0/0 | 8702 | 7 | 1 | 3 | 0 | 1 | 2 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0006 | 0/0 | 8712 | 7 | 6 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0007 | 0/0 | 8719 | 5 | 5 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0008 | 0/0 | 8712 | 4 | 1 | 0 | 0 | 0 | 3 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0009 | 0/0 | 8714 | 4 | 0 | 0 | 4 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0010 | 0/0 | 8708 | 4 | 0 | 1 | 0 | 0 | 3 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0011 | 0/0 | 8712 | 4 | 0 | 4 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0012 | 0/0 | 8701 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0013 | 0/0 | 8712 | 3 | 0 | 0 | 3 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0014 | 0/0 | 8708 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0015 | 0/0 | 8703 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0016 | 0/0 | 8702 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0017 | 0/0 | 8719 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0018 | 0/0 | 8719 | 3 | 1 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0019 | 0/1 | 8710 | 2 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0020 | 0/0 | 8714 | 2 | 2 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0021 | 0/0 | 8712 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0022 | 0/0 | 8712 | 2 | 1 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0023 | 0/0 | 8710 | 2 | 0 | 0 | 0 | 0 | 2 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0024 | 0/0 | 8714 | 2 | 0 | 0 | 2 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0025 | 0/0 | 8713 | 2 | 0 | 0 | 2 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0026 | 0/0 | 8711 | 2 | 2 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0027 | 0/0 | 8708 | 2 | 1 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0028 | 0/0 | 8717 | 2 | 1 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0029 | 0/0 | 8711 | 2 | 2 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0030 | 0/0 | 8714 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0031 | 0/0 | 8702 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0032 | 0/0 | 8712 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0033 | 0/0 | 8711 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0034 | 0/0 | 8714 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0035 | 0/0 | 8710 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0036 | 0/0 | 8712 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0037 | 0/0 | 8712 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0038 | 0/0 | 8700 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0039 | 0/0 | 8701 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0040 | 0/0 | 8715 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0041 | 0/0 | 8713 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0042 | 0/0 | 8714 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0043 | 0/0 | 8711 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0044 | 0/0 | 8712 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0045 | 0/0 | 8712 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0046 | 0/0 | 8712 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0047 | 0/0 | 8712 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0048 | 0/0 | 8712 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0049 | 0/0 | 8712 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0050 | 0/0 | 8714 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0051 | 0/0 | 8711 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0052 | 0/0 | 8707 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0053 | 0/0 | 8714 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0054 | 0/0 | 8711 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0055 | 0/0 | 8712 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0056 | 0/0 | 8712 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0057 | 0/0 | 8714 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0058 | 0/0 | 8710 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0059 | 0/0 | 8710 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0060 | 0/0 | 8712 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0061 | 0/0 | 8709 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0062 | 0/0 | 8711 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0063 | 0/0 | 8707 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0064 | 0/0 | 8702 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0065 | 0/0 | 8701 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0066 | 0/0 | 8720 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0067 | 0/0 | 8721 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0068 | 0/0 | 8721 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0069 | 0/0 | 8716 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0070 | 0/0 | 8710 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0071 | 0/0 | 8712 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0072 | 0/0 | 8714 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0073 | 0/0 | 8726 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0074 | 0/0 | 8728 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0075 | 0/0 | 8712 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0076 | 0/0 | 8711 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0077 | 0/0 | 8708 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0078 | 0/0 | 8714 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| t0079 | 0/0 | 8709 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1407 | 182 | 88 | 32 | 34 | 5 | 21 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0004 | 0/0 | 1407 | 2 | 0 | 0 | 2 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0005 | 0/0 | 1407 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0006 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0007 | 0/0 | 1407 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0002c0002 | 0/0 | 1407 | 6 | 0 | 3 | 3 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0003c0003 | 0/0 | 1407 | 4 | 0 | 2 | 0 | 1 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0004c0008 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 10118 | 33 | 3 | 9 | 12 | 3 | 5 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0002 | 0/0 | 10120 | 19 | 8 | 2 | 7 | 0 | 2 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0003 | 0/0 | 10115 | 8 | 8 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0004 | 0/0 | 10123 | 8 | 7 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0005 | 0/0 | 10108 | 7 | 1 | 3 | 0 | 1 | 2 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0006 | 0/0 | 10118 | 7 | 6 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0007 | 0/0 | 10125 | 5 | 5 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0008 | 0/0 | 10118 | 4 | 1 | 0 | 0 | 0 | 3 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0009 | 0/0 | 10120 | 3 | 0 | 0 | 3 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0010 | 0/0 | 10114 | 2 | 0 | 0 | 0 | 0 | 2 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0011 | 0/0 | 10118 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0012 | 0/0 | 10107 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0013 | 0/0 | 10118 | 3 | 0 | 0 | 3 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0014 | 0/0 | 10114 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0015 | 0/0 | 10109 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0016 | 0/0 | 10108 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0017 | 0/0 | 10125 | 3 | 3 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0018 | 0/0 | 10125 | 3 | 1 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0019 | 0/1 | 10116 | 2 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0020 | 0/0 | 10120 | 2 | 2 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0022 | 0/0 | 10118 | 2 | 1 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0023 | 0/0 | 10116 | 2 | 0 | 0 | 0 | 0 | 2 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0024 | 0/0 | 10120 | 2 | 0 | 0 | 2 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0025 | 0/0 | 10119 | 2 | 0 | 0 | 2 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0026 | 0/0 | 10117 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0027 | 0/0 | 10114 | 2 | 1 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0028 | 0/0 | 10123 | 2 | 1 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0029 | 0/0 | 10117 | 2 | 2 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0030 | 0/0 | 10120 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0031 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0033 | 0/0 | 10117 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0034 | 0/0 | 10120 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0035 | 0/0 | 10116 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0037 | 0/0 | 10118 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0038 | 0/0 | 10106 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0039 | 0/0 | 10107 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0040 | 0/0 | 10121 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0041 | 0/0 | 10119 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0042 | 0/0 | 10120 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0045 | 0/0 | 10118 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0046 | 0/0 | 10118 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0047 | 0/0 | 10118 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0048 | 0/0 | 10118 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0049 | 0/0 | 10118 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0050 | 0/0 | 10120 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0051 | 0/0 | 10117 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0052 | 0/0 | 10113 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0053 | 0/0 | 10120 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0054 | 0/0 | 10117 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0055 | 0/0 | 10118 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0057 | 0/0 | 10120 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0058 | 0/0 | 10116 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0060 | 0/0 | 10118 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0061 | 0/0 | 10115 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0062 | 0/0 | 10117 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0063 | 0/0 | 10113 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0064 | 0/0 | 10108 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0065 | 0/0 | 10107 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0066 | 0/0 | 10126 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0067 | 0/0 | 10127 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0068 | 0/0 | 10127 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0069 | 0/0 | 10122 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0070 | 0/0 | 10116 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0071 | 0/0 | 10118 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0073 | 0/0 | 10132 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0074 | 0/0 | 10134 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0075 | 0/0 | 10118 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0076 | 0/0 | 10117 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0077 | 0/0 | 10114 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0078 | 0/0 | 10120 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0001t0079 | 0/0 | 10115 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0004t0001 | 0/0 | 10118 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0004t0002 | 0/0 | 10120 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0005t0011 | 0/0 | 10118 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0006t0026 | 0/0 | 10117 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0006t0032 | 0/0 | 10118 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0001c0007t0072 | 0/0 | 10120 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0002c0002t0002 | 0/0 | 10120 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0002c0002t0021 | 0/0 | 10118 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0002c0002t0043 | 0/0 | 10117 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0002c0002t0044 | 0/0 | 10118 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0002c0002t0056 | 0/0 | 10118 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0003c0003t0010 | 0/0 | 10114 | 2 | 0 | 1 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0003c0003t0036 | 0/0 | 10118 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0003c0003t0059 | 0/0 | 10116 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| a0004c0008t0009 | 0/0 | 10120 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | copy fasta | chr22 | 46145526 | 46248755 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0008g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0009g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0010g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0010g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0013g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0014g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0014g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0014g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0015g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0016g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0016g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0017g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0017g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0018g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0018g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0018g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0019g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0019g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0020g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0020g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0022g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0022g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0023g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0023g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0024g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0024g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0025g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0025g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0026g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0027g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0027g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0028g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0028g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0029g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0029g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0030g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0031g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0033g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0034g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0035g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0037g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0038g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0039g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0040g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0041g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0042g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0045g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0046g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0047g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0048g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0049g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0050g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0051g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0052g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0053g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0054g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0055g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0057g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0058g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0060g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0061g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0062g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0063g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0064g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0065g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0066g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0067g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0068g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0069g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0070g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0071g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0073g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0074g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0075g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0076g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0077g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0078g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0001t0079g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0005t0011g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0005t0011g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0006t0026g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0006t0032g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0001c0007t0072g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0002c0002t0021g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0002c0002t0021g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0002c0002t0043g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0002c0002t0044g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0002c0002t0056g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0003c0003t0010g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0003c0003t0010g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0003c0003t0036g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0003c0003t0059g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| a0004c0008t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00438 | hp1 | a0001 | c0001 | t0048 | g0140 | EAS | CHS | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00639 | hp1 | a0003 | c0003 | t0059 | g0045 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01069 | hp2 | a0001 | c0005 | t0011 | g0014 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01071 | hp1 | a0001 | c0001 | t0030 | g0001 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01071 | hp2 | a0001 | c0005 | t0011 | g0016 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01106 | hp2 | a0001 | c0001 | t0034 | g0158 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01109 | hp1 | a0001 | c0001 | t0028 | g0127 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01109 | hp2 | a0001 | c0001 | t0047 | g0012 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01167 | hp1 | a0001 | c0001 | t0018 | g0186 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01167 | hp2 | a0001 | c0001 | t0051 | g0024 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01169 | hp1 | a0001 | c0001 | t0030 | g0001 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01169 | hp2 | a0001 | c0001 | t0018 | g0187 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0143 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01358 | hp1 | a0001 | c0001 | t0019 | g0088 | AMR | CLM | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01433 | hp1 | a0003 | c0003 | t0010 | g0043 | AMR | CLM | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01496 | hp1 | a0001 | c0001 | t0042 | g0105 | AMR | CLM | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01496 | hp2 | a0001 | c0001 | t0027 | g0002 | AMR | CLM | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01516 | hp2 | a0003 | c0003 | t0036 | g0013 | EUR | IBS | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01884 | hp1 | a0001 | c0001 | t0064 | g0159 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0077 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01891 | hp1 | a0001 | c0006 | t0026 | g0142 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01928 | hp1 | a0002 | c0002 | t0021 | g0035 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01934 | hp2 | a0001 | c0001 | t0011 | g0094 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01943 | hp1 | a0002 | c0002 | t0043 | g0111 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01943 | hp2 | a0001 | c0001 | t0066 | g0050 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01952 | hp2 | a0002 | c0002 | t0021 | g0114 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01975 | hp1 | a0001 | c0007 | t0072 | g0033 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01975 | hp2 | a0001 | c0001 | t0052 | g0066 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02040 | hp2 | a0001 | c0001 | t0013 | g0085 | EAS | KHV | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02055 | hp1 | a0001 | c0001 | t0041 | g0190 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02071 | hp1 | a0001 | c0001 | t0009 | g0173 | EAS | KHV | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02145 | hp1 | a0001 | c0001 | t0054 | g0089 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02145 | hp2 | a0001 | c0001 | t0029 | g0162 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CDX | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02165 | hp2 | a0001 | c0001 | t0055 | g0155 | EAS | CDX | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0067 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02257 | hp2 | a0001 | c0001 | t0015 | g0136 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0027 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02258 | hp2 | a0001 | c0001 | t0078 | g0196 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02273 | hp1 | a0001 | c0001 | t0071 | g0010 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0061 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0034 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02451 | hp1 | a0001 | c0001 | t0067 | g0022 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02523 | hp1 | a0001 | c0001 | t0025 | g0056 | EAS | KHV | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02523 | hp2 | a0001 | c0001 | t0025 | g0058 | EAS | KHV | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02572 | hp1 | a0001 | c0001 | t0015 | g0019 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02572 | hp2 | a0001 | c0001 | t0057 | g0157 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0134 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0160 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0197 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02630 | hp2 | a0001 | c0001 | t0065 | g0047 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0153 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02698 | hp2 | a0001 | c0001 | t0037 | g0064 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0123 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0046 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02818 | hp2 | a0001 | c0001 | t0038 | g0126 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0083 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02886 | hp2 | a0001 | c0001 | t0061 | g0188 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02895 | hp1 | a0001 | c0001 | t0074 | g0112 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0120 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02897 | hp1 | a0001 | c0001 | t0060 | g0129 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02965 | hp1 | a0001 | c0001 | t0029 | g0003 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02965 | hp2 | a0001 | c0001 | t0079 | g0107 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03017 | hp1 | a0001 | c0001 | t0045 | g0059 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03017 | hp2 | a0001 | c0001 | t0008 | g0183 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0048 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0100 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03130 | hp1 | a0001 | c0001 | t0020 | g0128 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0178 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03209 | hp1 | a0001 | c0001 | t0040 | g0074 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03225 | hp1 | a0001 | c0006 | t0032 | g0132 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03239 | hp2 | a0001 | c0001 | t0010 | g0182 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03486 | hp1 | a0001 | c0001 | t0027 | g0156 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03486 | hp2 | a0001 | c0001 | t0070 | g0168 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03491 | hp1 | a0001 | c0001 | t0031 | g0198 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03491 | hp2 | a0001 | c0001 | t0053 | g0116 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0199 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03516 | hp1 | a0001 | c0001 | t0077 | g0004 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03540 | hp2 | a0001 | c0001 | t0073 | g0042 | AFR | GWD | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03579 | hp1 | a0001 | c0001 | t0063 | g0099 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03704 | hp1 | a0001 | c0001 | t0010 | g0040 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03704 | hp2 | a0001 | c0001 | t0023 | g0081 | SAS | PJL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03831 | hp1 | a0001 | c0001 | t0023 | g0176 | SAS | BEB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03834 | hp1 | a0001 | c0001 | t0035 | g0163 | SAS | BEB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0109 | SAS | BEB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG04184 | hp2 | a0003 | c0003 | t0010 | g0031 | SAS | BEB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18522 | hp1 | a0001 | c0001 | t0075 | g0006 | AFR | YRI | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18522 | hp2 | a0001 | c0001 | t0033 | g0133 | AFR | YRI | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18906 | hp1 | a0001 | c0001 | t0076 | g0030 | AFR | YRI | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18906 | hp2 | a0001 | c0001 | t0018 | g0097 | AFR | YRI | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18948 | hp1 | a0002 | c0002 | t0056 | g0179 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18948 | hp2 | a0001 | c0001 | t0024 | g0180 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18952 | hp2 | a0001 | c0001 | t0009 | g0091 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18966 | hp1 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18974 | hp1 | a0001 | c0001 | t0049 | g0092 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18974 | hp2 | a0001 | c0001 | t0013 | g0192 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18993 | hp1 | a0004 | c0008 | t0009 | g0146 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18993 | hp2 | a0001 | c0001 | t0009 | g0175 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19004 | hp1 | a0001 | c0001 | t0050 | g0078 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19004 | hp2 | a0001 | c0001 | t0046 | g0154 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19030 | hp1 | a0001 | c0001 | t0069 | g0161 | AFR | LWK | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0177 | AFR | LWK | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | LWK | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0137 | AFR | LWK | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19070 | hp1 | a0001 | c0001 | t0024 | g0181 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19070 | hp2 | a0001 | c0004 | t0002 | g0113 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19085 | hp1 | a0001 | c0004 | t0001 | g0055 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA19085 | hp2 | a0002 | c0002 | t0044 | g0023 | EAS | JPT | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ASW | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ASW | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0130 | EUR | TSI | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA20805 | hp2 | a0001 | c0001 | t0022 | g0076 | EUR | TSI | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | GIH | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0115 | SAS | GIH | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0152 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0167 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02486 | hp1 | a0001 | c0001 | t0016 | g0194 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02486 | hp2 | a0001 | c0001 | t0039 | g0041 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG02559 | hp2 | a0001 | c0001 | t0062 | g0026 | AFR | ACB | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG03471 | hp2 | a0001 | c0001 | t0068 | g0119 | AFR | MSL | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG06807 | hp1 | a0001 | c0001 | t0017 | g0062 | AFR | USA | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | USA | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | USA | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA21309 | hp1 | a0001 | c0001 | t0028 | g0118 | AFR | LWK | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| NA21309 | hp2 | a0001 | c0001 | t0058 | g0079 | AFR | LWK | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0019 | g0141 | REF | REF | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0044 | REF | REF | PPARA_chr22_46145526_46248755 | PPARA | chr22 | 46145526 | 46248755 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46218377
|
C | G | 1 | a0003 | 4 | HG00639.hp1 HG01433.hp1 HG01516.hp2 others(1): Show |
missense_variant | MODERATE | c.484C>G | p.Leu162Val | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/9 | 820/10118 | 484/1407 | 162/468 | chr22 | 46218377 | ||
| chr22:46219983
|
T | C | 1 | a0002 | 6 | HG01928.hp1 HG01943.hp1 HG01952.hp2 others(3): Show |
missense_variant | MODERATE | c.680T>C | p.Val227Ala | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/9 | 1016/10118 | 680/1407 | 227/468 | chr22 | 46219983 | ||
| chr22:46235157
|
G | A | 1 | a0004 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1184G>A | p.Gly395Glu | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1520/10118 | 1184/1407 | 395/468 | chr22 | 46235157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46215256
|
T | C | 1 | a0001c0004 | 2 | NA19070.hp2 NA19085.hp1 |
synonymous_variant | LOW | c.292T>C | p.Leu98Leu | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/9 | 628/10118 | 292/1407 | 98/468 | chr22 | 46215256 | ||
| chr22:46219813
|
G | A | 1 | a0001c0007 | 1 | HG01975.hp1 | splice_region_variant&synonymous_variant | LOW | c.510G>A | p.Ala170Ala | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/9 | 846/10118 | 510/1407 | 170/468 | chr22 | 46219813 | ||
| chr22:46220008
|
C | T | 1 | a0001c0006 | 2 | HG01891.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.705C>T | p.Asn235Asn | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/9 | 1041/10118 | 705/1407 | 235/468 | chr22 | 46220008 | ||
| chr22:46231950
|
C | T | 1 | a0001c0005 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.870C>T | p.Phe290Phe | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/9 | 1206/10118 | 870/1407 | 290/468 | chr22 | 46231950 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46150544
|
CGGCGGGG others(3): Show |
C | 1 | a0001c0001t0031 | 1 | HG03491.hp1 | 5_prime_UTR_variant | MODIFIER | c.-316_-307delGCGGGG others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/9 | 47829 | INFO_REALIGN_3_PRIME | chr22 | 46150544 | ||||
| chr22:46150577
|
G | A | 2 | a0001c0001t0033a0001c0006t0032 | 2 | HG03225.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-285G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/9 | 47807 | chr22 | 46150577 | |||||
| chr22:46235554
|
C | A | 1 | a0001c0001t0019 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*174C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 174 | chr22 | 46235554 | |||||
| chr22:46235613
|
A | G | 3 | a0001c0001t0077a0001c0001t0078a0001c0001t0079 | 3 | HG02258.hp2 HG02965.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*233A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 233 | chr22 | 46235613 | |||||
| chr22:46235763
|
A | G | 1 | a0001c0001t0030 | 2 | HG01071.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*383A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 383 | chr22 | 46235763 | |||||
| chr22:46235790
|
T | C | 1 | a0001c0001t0020 | 2 | HG03130.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 410 | chr22 | 46235790 | |||||
| chr22:46236263
|
A | C | 5 | a0001c0001t0007a0001c0001t0073a0001c0001t0074others(2): Show | 9 | HG02615.hp1 HG02622.hp1 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*883A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 883 | chr22 | 46236263 | |||||
| chr22:46236562
|
C | T | 4 | a0001c0001t0011a0001c0001t0071a0001c0005t0011others(1): Show | 6 | HG01069.hp2 HG01071.hp2 HG01934.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1182C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1182 | chr22 | 46236562 | |||||
| chr22:46236647
|
T | C | 2 | a0001c0001t0073a0001c0001t0074 | 2 | HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1267T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1267 | chr22 | 46236647 | |||||
| chr22:46236692
|
G | A | 3 | a0001c0001t0008a0001c0001t0031a0001c0001t0034 | 6 | HG01106.hp2 HG02109.hp2 HG03017.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1312G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1312 | chr22 | 46236692 | |||||
| chr22:46236699
|
A | G | 2 | a0001c0001t0073a0001c0001t0074 | 2 | HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1319A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1319 | chr22 | 46236699 | |||||
| chr22:46236905
|
C | T | 1 | a0001c0001t0019 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1525C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1525 | chr22 | 46236905 | |||||
| chr22:46237097
|
G | A | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1717G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1717 | chr22 | 46237097 | |||||
| chr22:46237130
|
G | A | 1 | a0001c0001t0035 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1750G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1750 | chr22 | 46237130 | |||||
| chr22:46237140
|
G | C | 1 | a0003c0003t0036 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1760 | chr22 | 46237140 | |||||
| chr22:46237205
|
G | A | 1 | a0001c0001t0037 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1825G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1825 | chr22 | 46237205 | |||||
| chr22:46237251
|
AAGTT | A | 3 | a0001c0001t0012a0001c0001t0038a0001c0001t0039 | 5 | HG02486.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1874_*1877delTTAG | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1874 | INFO_REALIGN_3_PRIME | chr22 | 46237251 | ||||
| chr22:46237302
|
G | T | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0017others(9): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1922G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1922 | chr22 | 46237302 | |||||
| chr22:46237366
|
G | C | 1 | a0001c0001t0077 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1986G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 1986 | chr22 | 46237366 | |||||
| chr22:46237424
|
C | G | 3 | a0001c0001t0016a0001c0001t0064a0001c0001t0065 | 5 | HG01884.hp1 HG02258.hp1 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2044C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2044 | chr22 | 46237424 | |||||
| chr22:46237458
|
C | T | 2 | a0001c0001t0027a0001c0001t0035 | 3 | HG01496.hp2 HG03486.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2078C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2078 | chr22 | 46237458 | |||||
| chr22:46237474
|
A | T | 44 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(41): Show | 93 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2094A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2094 | chr22 | 46237474 | |||||
| chr22:46237577
|
G | A | 1 | a0001c0001t0071 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2197G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2197 | chr22 | 46237577 | |||||
| chr22:46237608
|
G | A | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2228G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2228 | chr22 | 46237608 | |||||
| chr22:46237610
|
C | CA | 23 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(20): Show | 44 | HG00639.hp1 HG01243.hp1 HG01358.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2246dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2247 | INFO_REALIGN_3_PRIME | chr22 | 46237610 | ||||
| chr22:46237654
|
C | T | 4 | a0001c0001t0003a0001c0001t0060a0001c0001t0061others(1): Show | 11 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2274C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2274 | chr22 | 46237654 | |||||
| chr22:46237669
|
C | T | 1 | a0001c0001t0030 | 2 | HG01071.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2289C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2289 | chr22 | 46237669 | |||||
| chr22:46237885
|
G | A | 44 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(41): Show | 93 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2505G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2505 | chr22 | 46237885 | |||||
| chr22:46238199
|
T | C | 4 | a0001c0001t0003a0001c0001t0060a0001c0001t0061others(1): Show | 11 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2819T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 2819 | chr22 | 46238199 | |||||
| chr22:46238491
|
C | T | 3 | a0001c0001t0012a0001c0001t0038a0001c0001t0039 | 5 | HG02486.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3111C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3111 | chr22 | 46238491 | |||||
| chr22:46238619
|
C | T | 1 | a0001c0001t0064 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3239C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3239 | chr22 | 46238619 | |||||
| chr22:46238834
|
AG | A | 6 | a0001c0001t0012a0001c0001t0015a0001c0001t0027others(3): Show | 11 | HG01496.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3457delG | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3457 | INFO_REALIGN_3_PRIME | chr22 | 46238834 | ||||
| chr22:46238888
|
G | A | 2 | a0001c0001t0073a0001c0001t0074 | 2 | HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3508G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3508 | chr22 | 46238888 | |||||
| chr22:46238945
|
C | T | 1 | a0001c0001t0039 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3565C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3565 | chr22 | 46238945 | |||||
| chr22:46238982
|
G | A | 4 | a0001c0001t0028a0001c0001t0066a0001c0001t0067others(1): Show | 5 | HG01109.hp1 HG01943.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3602G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3602 | chr22 | 46238982 | |||||
| chr22:46239166
|
G | A | 1 | a0001c0001t0066 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3786G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3786 | chr22 | 46239166 | |||||
| chr22:46239199
|
C | T | 1 | a0002c0002t0056 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3819C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3819 | chr22 | 46239199 | |||||
| chr22:46239299
|
G | A | 1 | a0001c0001t0075 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3919G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 3919 | chr22 | 46239299 | |||||
| chr22:46239424
|
T | A | 2 | a0002c0002t0021a0002c0002t0043 | 3 | HG01928.hp1 HG01943.hp1 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4044T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 4044 | chr22 | 46239424 | |||||
| chr22:46239625
|
C | T | 1 | a0001c0001t0015 | 3 | HG02257.hp2 HG02572.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4245C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 4245 | chr22 | 46239625 | |||||
| chr22:46239702
|
G | A | 12 | a0001c0001t0004a0001c0001t0007a0001c0001t0017others(9): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4322G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 4322 | chr22 | 46239702 | |||||
| chr22:46239779
|
G | A | 2 | a0001c0001t0014a0001c0001t0063 | 4 | HG01884.hp2 HG02818.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4399G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 4399 | chr22 | 46239779 | |||||
| chr22:46239911
|
A | G | 1 | a0001c0001t0055 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4531A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 4531 | chr22 | 46239911 | |||||
| chr22:46240297
|
A | G | 2 | a0001c0001t0027a0001c0001t0035 | 3 | HG01496.hp2 HG03486.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4917A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 4917 | chr22 | 46240297 | |||||
| chr22:46240573
|
C | T | 16 | a0001c0001t0004a0001c0001t0007a0001c0001t0012others(13): Show | 37 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5193C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5193 | chr22 | 46240573 | |||||
| chr22:46240678
|
G | A | 1 | a0001c0001t0029 | 2 | HG02145.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5298G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5298 | chr22 | 46240678 | |||||
| chr22:46240769
|
TC | T | 6 | a0001c0001t0003a0001c0001t0060a0001c0001t0061others(3): Show | 13 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5390delC | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5390 | chr22 | 46240769 | |||||
| chr22:46240796
|
T | C | 1 | a0001c0001t0078 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5416T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5416 | chr22 | 46240796 | |||||
| chr22:46240906
|
G | A | 2 | a0001c0001t0077a0001c0001t0079 | 2 | HG02965.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5526G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5526 | chr22 | 46240906 | |||||
| chr22:46241033
|
C | T | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5653C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5653 | chr22 | 46241033 | |||||
| chr22:46241079
|
G | A | 6 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(3): Show | 16 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5699G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5699 | chr22 | 46241079 | |||||
| chr22:46241140
|
T | C | 2 | a0001c0001t0027a0001c0001t0035 | 3 | HG01496.hp2 HG03486.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5760T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5760 | chr22 | 46241140 | |||||
| chr22:46241154
|
A | T | 1 | a0001c0001t0070 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5774A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5774 | chr22 | 46241154 | |||||
| chr22:46241297
|
C | T | 1 | a0001c0001t0054 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5917C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5917 | chr22 | 46241297 | |||||
| chr22:46241335
|
A | G | 1 | a0001c0001t0053 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5955A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5955 | chr22 | 46241335 | |||||
| chr22:46241342
|
T | C | 15 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(12): Show | 38 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*5962T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5962 | chr22 | 46241342 | |||||
| chr22:46241357
|
G | A | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(14): Show | 44 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5977G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5977 | chr22 | 46241357 | |||||
| chr22:46241375
|
T | C | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5995T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 5995 | chr22 | 46241375 | |||||
| chr22:46241538
|
CAG | C | 2 | a0001c0001t0077a0001c0001t0079 | 2 | HG02965.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6160_*6161delGA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6160 | INFO_REALIGN_3_PRIME | chr22 | 46241538 | ||||
| chr22:46241548
|
A | G | 3 | a0001c0001t0006a0001c0001t0033a0001c0006t0032 | 9 | HG01243.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6168A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6168 | chr22 | 46241548 | |||||
| chr22:46241614
|
G | A | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6234G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6234 | chr22 | 46241614 | |||||
| chr22:46241749
|
T | C | 4 | a0001c0001t0012a0001c0001t0015a0001c0001t0038others(1): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6369T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6369 | chr22 | 46241749 | |||||
| chr22:46241770
|
A | T | 2 | a0001c0001t0027a0001c0001t0035 | 3 | HG01496.hp2 HG03486.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6390A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6390 | chr22 | 46241770 | |||||
| chr22:46241876
|
T | C | 1 | a0001c0001t0045 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6496T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6496 | chr22 | 46241876 | |||||
| chr22:46241882
|
A | C | 4 | a0001c0001t0004a0001c0001t0018a0001c0001t0029others(1): Show | 14 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6502A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6502 | chr22 | 46241882 | |||||
| chr22:46241901
|
G | C | 1 | a0001c0001t0046 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6521G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6521 | chr22 | 46241901 | |||||
| chr22:46241913
|
GA | G | 43 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(40): Show | 86 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*6551delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6551 | INFO_REALIGN_3_PRIME | chr22 | 46241913 | ||||
| chr22:46241913
|
GAA | G | 5 | a0001c0001t0033a0001c0001t0038a0001c0001t0066others(2): Show | 5 | HG01943.hp2 HG02818.hp2 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6550_*6551delAA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6550 | INFO_REALIGN_3_PRIME | chr22 | 46241913 | ||||
| chr22:46241913
|
GAAA | G | 3 | a0001c0001t0003a0001c0001t0061a0001c0001t0062 | 10 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6549_*6551delAAA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6549 | INFO_REALIGN_3_PRIME | chr22 | 46241913 | ||||
| chr22:46241930
|
A | G | 6 | a0001c0001t0009a0001c0001t0010a0001c0001t0035others(3): Show | 10 | HG00639.hp1 HG01433.hp1 HG02071.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6550A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6550 | chr22 | 46241930 | |||||
| chr22:46242189
|
C | A | 1 | a0001c0001t0047 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6809C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6809 | chr22 | 46242189 | |||||
| chr22:46242220
|
G | A | 25 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(22): Show | 47 | HG00639.hp1 HG01243.hp1 HG01358.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*6840G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6840 | chr22 | 46242220 | |||||
| chr22:46242231
|
C | G | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(4): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6851C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6851 | chr22 | 46242231 | |||||
| chr22:46242260
|
G | C | 1 | a0001c0001t0035 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6880G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6880 | chr22 | 46242260 | |||||
| chr22:46242261
|
A | G | 1 | a0001c0001t0047 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6881A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6881 | chr22 | 46242261 | |||||
| chr22:46242262
|
C | A | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(4): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6882C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6882 | chr22 | 46242262 | |||||
| chr22:46242274
|
G | A | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(4): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6894G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6894 | chr22 | 46242274 | |||||
| chr22:46242314
|
G | A | 5 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(2): Show | 15 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6934G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6934 | chr22 | 46242314 | |||||
| chr22:46242319
|
C | G | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(4): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6939C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6939 | chr22 | 46242319 | |||||
| chr22:46242332
|
G | A | 1 | a0001c0001t0061 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6952G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 6952 | chr22 | 46242332 | |||||
| chr22:46242401
|
C | T | 32 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(29): Show | 64 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*7021C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7021 | chr22 | 46242401 | |||||
| chr22:46242415
|
A | G | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(4): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7035A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7035 | chr22 | 46242415 | |||||
| chr22:46242468
|
A | G | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(4): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7088A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7088 | chr22 | 46242468 | |||||
| chr22:46242508
|
C | T | 1 | a0001c0001t0019 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7128C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7128 | chr22 | 46242508 | |||||
| chr22:46242523
|
CT | C | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(4): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7145delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7145 | INFO_REALIGN_3_PRIME | chr22 | 46242523 | ||||
| chr22:46242589
|
C | T | 7 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(4): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7209C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7209 | chr22 | 46242589 | |||||
| chr22:46242643
|
A | G | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7263A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7263 | chr22 | 46242643 | |||||
| chr22:46242716
|
C | T | 2 | a0001c0001t0024a0001c0001t0050 | 3 | NA18948.hp2 NA19004.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7336C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7336 | chr22 | 46242716 | |||||
| chr22:46242728
|
C | T | 6 | a0001c0001t0012a0001c0001t0015a0001c0001t0038others(3): Show | 10 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7348C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7348 | chr22 | 46242728 | |||||
| chr22:46242729
|
GTGCA | G | 3 | a0001c0001t0012a0001c0001t0038a0001c0001t0039 | 5 | HG02486.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7350_*7353delTGCA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7350 | chr22 | 46242729 | |||||
| chr22:46242729
|
GTGCACA | G | 1 | a0001c0001t0015 | 3 | HG02257.hp2 HG02572.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7350_*7355delTGCA others(2): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7350 | chr22 | 46242729 | |||||
| chr22:46242729
|
GTGCACAC others(1): Show |
G | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7350_*7357delTGCA others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7350 | chr22 | 46242729 | |||||
| chr22:46242730
|
T | C | 3 | a0001c0001t0070a0001c0001t0073a0001c0001t0074 | 3 | HG02895.hp1 HG03486.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7350T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7350 | chr22 | 46242730 | |||||
| chr22:46242731
|
G | GCA | 18 | a0001c0001t0002a0001c0001t0009a0001c0001t0020others(15): Show | 42 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*7380_*7381dupCA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7382 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242731
|
G | GCACACA | 3 | a0001c0001t0004a0001c0001t0028a0001c0001t0069 | 11 | HG01109.hp1 HG01433.hp2 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7376_*7381dupCACA others(2): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7382 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242731
|
G | GCACACAC others(1): Show |
3 | a0001c0001t0007a0001c0001t0017a0001c0001t0018 | 11 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7374_*7381dupCACA others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7382 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242731
|
G | GCACACAC others(3): Show |
3 | a0001c0001t0066a0001c0001t0067a0001c0001t0068 | 3 | HG01943.hp2 HG02451.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7372_*7381dupCACA others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7382 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242731
|
G | GCGCGCGC others(9): Show |
1 | a0001c0001t0073 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7352_*7353insGCGC others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7353 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242731
|
G | GCGCGCGC others(11): Show |
1 | a0001c0001t0074 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7352_*7353insGCGC others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7353 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242731
|
GCA | G | 5 | a0001c0001t0019a0001c0001t0023a0001c0001t0027others(2): Show | 8 | HG00639.hp1 HG01358.hp1 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7380_*7381delCA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7380 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242731
|
GCACA | G | 5 | a0001c0001t0010a0001c0001t0014a0001c0001t0052others(2): Show | 9 | HG01433.hp1 HG01884.hp2 HG01975.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7378_*7381delCACA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7378 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242731
|
GCACACAC others(3): Show |
G | 3 | a0001c0001t0016a0001c0001t0064a0001c0001t0065 | 5 | HG01884.hp1 HG02258.hp1 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7372_*7381delCACA others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7372 | INFO_REALIGN_3_PRIME | chr22 | 46242731 | ||||
| chr22:46242735
|
A | G | 4 | a0001c0001t0012a0001c0001t0027a0001c0001t0038others(1): Show | 7 | HG01496.hp2 HG02486.hp2 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7355A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7355 | chr22 | 46242735 | |||||
| chr22:46242737
|
A | G | 4 | a0001c0001t0012a0001c0001t0015a0001c0001t0038others(1): Show | 8 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7357A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7357 | chr22 | 46242737 | |||||
| chr22:46242739
|
A | G | 5 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(2): Show | 15 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*7359A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7359 | chr22 | 46242739 | |||||
| chr22:46242741
|
A | G | 2 | a0001c0001t0005a0001c0001t0015 | 10 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7361A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7361 | chr22 | 46242741 | |||||
| chr22:46242743
|
A | G | 1 | a0001c0001t0015 | 3 | HG02257.hp2 HG02572.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7363A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7363 | chr22 | 46242743 | |||||
| chr22:46242762
|
G | C | 1 | a0001c0001t0076 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7382G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7382 | chr22 | 46242762 | |||||
| chr22:46242773
|
C | A | 2 | a0001c0001t0022a0001c0001t0051 | 3 | HG01167.hp2 HG02257.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7393C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7393 | chr22 | 46242773 | |||||
| chr22:46242801
|
A | G | 1 | a0001c0001t0065 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7421A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7421 | chr22 | 46242801 | |||||
| chr22:46242973
|
C | A | 1 | a0001c0001t0035 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7593C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7593 | chr22 | 46242973 | |||||
| chr22:46242994
|
A | G | 1 | a0001c0001t0049 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7614A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7614 | chr22 | 46242994 | |||||
| chr22:46243025
|
G | T | 2 | a0001c0001t0077a0001c0001t0079 | 2 | HG02965.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7645G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7645 | chr22 | 46243025 | |||||
| chr22:46243151
|
G | A | 2 | a0001c0001t0073a0001c0001t0074 | 2 | HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7771G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7771 | chr22 | 46243151 | |||||
| chr22:46243284
|
A | T | 2 | a0001c0001t0073a0001c0001t0074 | 2 | HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7904A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7904 | chr22 | 46243284 | |||||
| chr22:46243301
|
T | C | 2 | a0001c0001t0018a0001c0001t0029 | 5 | HG01167.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7921T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7921 | chr22 | 46243301 | |||||
| chr22:46243358
|
T | G | 1 | a0001c0001t0048 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7978T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 7978 | chr22 | 46243358 | |||||
| chr22:46243463
|
G | A | 1 | a0001c0007t0072 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8083G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 8083 | chr22 | 46243463 | |||||
| chr22:46243489
|
G | A | 2 | a0001c0001t0005a0001c0006t0032 | 8 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8109G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 8109 | chr22 | 46243489 | |||||
| chr22:46243491
|
A | G | 2 | a0001c0001t0073a0001c0001t0074 | 2 | HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8111A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 8111 | chr22 | 46243491 | |||||
| chr22:46243560
|
A | T | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8180A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 8180 | chr22 | 46243560 | |||||
| chr22:46243564
|
T | A | 15 | a0001c0001t0004a0001c0001t0007a0001c0001t0012others(12): Show | 36 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*8184T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 8184 | chr22 | 46243564 | |||||
| chr22:46243565
|
A | T | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8185A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 8185 | chr22 | 46243565 | |||||
| chr22:46243599
|
G | C | 1 | a0001c0001t0024 | 2 | NA18948.hp2 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8219G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 8219 | chr22 | 46243599 | |||||
| chr22:46243716
|
G | C | 1 | a0002c0002t0056 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8336G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 9/9 | 8336 | chr22 | 46243716 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46150660
|
GGGGC | G | 12 | a0001c0001t0001g0008a0001c0001t0005g0007a0001c0001t0005g0009others(9): Show | 12 | HG00738.hp2 HG01106.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-210+28_-210+31del others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 46150660 | |||||
| chr22:46150704
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-210+52G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | chr22 | 46150704 | ||||||
| chr22:46150734
|
G | A | 1 | a0001c0001t0015g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-210+82G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | chr22 | 46150734 | ||||||
| chr22:46150765
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0007g0020 | 2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-210+113G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | chr22 | 46150765 | ||||||
| chr22:46150870
|
CCGAGGAC others(5): Show |
C | 9 | a0001c0001t0001g0008a0001c0001t0005g0007a0001c0001t0005g0009others(6): Show | 9 | HG00738.hp2 HG01106.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-210+224_-210+235d others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 46150870 | |||||
| chr22:46150981
|
G | A | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-210+329G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | chr22 | 46150981 | ||||||
| chr22:46151124
|
CCTCCAGG others(3): Show |
C | 3 | a0001c0001t0002g0195a0001c0001t0006g0197a0001c0001t0078g0196 | 3 | HG02258.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-210+477_-210+486d others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 46151124 | |||||
| chr22:46151219
|
G | A | 1 | a0001c0001t0007g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-210+567G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | chr22 | 46151219 | ||||||
| chr22:46151778
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0016g0194 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-209-110C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 1/8 | chr22 | 46151778 | ||||||
| chr22:46152025
|
G | T | 1 | a0001c0001t0013g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-127+55G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152025 | ||||||
| chr22:46152122
|
G | A | 1 | a0002c0002t0044g0023 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-127+152G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152122 | ||||||
| chr22:46152132
|
A | AT | 34 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 34 | HG00099.hp1 HG01071.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.-127+186dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46152132 | |||||
| chr22:46152132
|
AT | A | 9 | a0001c0001t0003g0025a0001c0001t0005g0028a0001c0001t0006g0029others(6): Show | 9 | HG01069.hp1 HG01167.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+186delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46152132 | |||||
| chr22:46152167
|
C | T | 1 | a0002c0002t0002g0164 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-127+197C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152167 | ||||||
| chr22:46152284
|
G | T | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-127+314G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152284 | ||||||
| chr22:46152663
|
C | T | 1 | a0001c0001t0035g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-127+693C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152663 | ||||||
| chr22:46152697
|
A | G | 18 | a0001c0001t0002g0185a0001c0001t0002g0189a0001c0001t0002g0191others(15): Show | 18 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-127+727A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152697 | ||||||
| chr22:46152815
|
G | A | 1 | a0003c0003t0010g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-127+845G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152815 | ||||||
| chr22:46152864
|
C | T | 1 | a0001c0001t0055g0155 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-127+894C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152864 | ||||||
| chr22:46152868
|
T | A | 4 | a0001c0001t0002g0032a0001c0001t0011g0034a0001c0007t0072g0033others(1): Show | 4 | HG01928.hp1 HG01952.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+898T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152868 | ||||||
| chr22:46152887
|
C | T | 7 | a0001c0001t0002g0185a0001c0001t0002g0189a0001c0001t0002g0191others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-127+917C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152887 | ||||||
| chr22:46152960
|
T | C | 18 | a0001c0001t0002g0185a0001c0001t0002g0189a0001c0001t0002g0191others(15): Show | 18 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-127+990T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46152960 | ||||||
| chr22:46153009
|
C | A | 2 | a0001c0001t0006g0029a0001c0001t0076g0030 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+1039C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153009 | ||||||
| chr22:46153072
|
C | A | 1 | a0001c0001t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-127+1102C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153072 | ||||||
| chr22:46153163
|
C | CT | 38 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0148others(35): Show | 38 | HG00438.hp1 HG00738.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-127+1216dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46153163 | |||||
| chr22:46153163
|
C | CTT | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0184others(12): Show | 15 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.-127+1215_-127+121 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46153163 | |||||
| chr22:46153246
|
C | T | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-127+1276C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153246 | ||||||
| chr22:46153262
|
C | T | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-127+1292C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153262 | ||||||
| chr22:46153268
|
C | T | 1 | a0001c0001t0006g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-127+1298C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153268 | ||||||
| chr22:46153269
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0007g0020 | 2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-127+1299G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153269 | ||||||
| chr22:46153307
|
T | G | 2 | a0001c0001t0006g0029a0001c0001t0076g0030 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+1337T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153307 | ||||||
| chr22:46153451
|
G | A | 4 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0007g0036others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+1481G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153451 | ||||||
| chr22:46153488
|
G | C | 8 | a0001c0001t0002g0039a0001c0001t0002g0185a0001c0001t0002g0189others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+1518G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153488 | ||||||
| chr22:46153502
|
G | C | 1 | a0001c0001t0010g0040 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-127+1532G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153502 | ||||||
| chr22:46153589
|
C | T | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-127+1619C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46153589 | ||||||
| chr22:46154011
|
T | A | 4 | a0001c0001t0002g0195a0001c0001t0006g0197a0001c0001t0067g0022others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+2041T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46154011 | ||||||
| chr22:46154203
|
A | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 15 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.-127+2233A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46154203 | ||||||
| chr22:46154271
|
T | C | 4 | a0001c0001t0002g0195a0001c0001t0006g0197a0001c0001t0067g0022others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+2301T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46154271 | ||||||
| chr22:46154412
|
C | G | 163 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.-127+2442C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46154412 | ||||||
| chr22:46154987
|
TTAAAAAA others(6): Show |
T | 1 | a0001c0001t0015g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-127+3018_-127+303 others(17): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46154987 | ||||||
| chr22:46154988
|
T | TA | 18 | a0001c0001t0001g0080a0001c0001t0001g0193a0001c0001t0002g0075others(15): Show | 18 | HG00597.hp1 HG00597.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-127+3057dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
T | TAA | 16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(13): Show | 16 | HG00099.hp2 HG00639.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-127+3056_-127+305 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
T | TAAAA | 7 | a0001c0001t0003g0144a0001c0001t0020g0178a0001c0001t0027g0156others(4): Show | 7 | HG01106.hp2 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127+3054_-127+305 others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
T | TAAAAAAA others(9): Show |
2 | a0001c0001t0006g0134a0001c0001t0073g0042 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-127+3042_-127+305 others(20): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0039g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-127+3040_-127+305 others(22): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TA | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0110a0001c0001t0001g0148others(34): Show | 38 | HG01069.hp1 HG01071.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.-127+3057delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAA | T | 23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0122others(20): Show | 23 | HG00099.hp1 HG01071.hp2 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.-127+3056_-127+305 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAA | T | 6 | a0001c0001t0012g0137a0001c0001t0020g0128a0001c0001t0028g0127others(3): Show | 6 | HG01069.hp2 HG01109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127+3055_-127+305 others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAA | T | 5 | a0001c0001t0004g0049a0001c0001t0004g0051a0001c0001t0005g0130others(2): Show | 5 | HG01943.hp2 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127+3054_-127+305 others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAA | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG01106.hp1 HG01358.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-127+3052_-127+305 others(10): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAAA | T | 9 | a0001c0001t0001g0138a0001c0001t0002g0166a0001c0001t0003g0021others(6): Show | 9 | HG00738.hp2 HG01109.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+3051_-127+305 others(11): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAAA others(1): Show |
T | 10 | a0001c0001t0001g0057a0001c0001t0001g0139a0001c0001t0002g0054others(7): Show | 10 | HG00438.hp1 HG00738.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-127+3050_-127+305 others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAAA others(3): Show |
T | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-127+3048_-127+305 others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-127+3046_-127+305 others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0013g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-127+3045_-127+305 others(17): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAAA others(14): Show |
T | 11 | a0001c0001t0002g0063a0001c0001t0004g0060a0001c0001t0006g0029others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.-127+3037_-127+305 others(25): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAAA others(16): Show |
T | 4 | a0001c0001t0002g0195a0001c0001t0006g0197a0001c0001t0029g0162others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+3035_-127+305 others(27): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46154988
|
TAAAAAAA others(17): Show |
T | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-127+3034_-127+305 others(28): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46154988 | |||||
| chr22:46155021
|
A | C | 20 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(17): Show | 20 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-127+3051A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155021 | ||||||
| chr22:46155028
|
C | A | 1 | a0001c0001t0037g0064 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-127+3058C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155028 | ||||||
| chr22:46155064
|
T | C | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-127+3094T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155064 | ||||||
| chr22:46155088
|
C | A | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-127+3118C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155088 | ||||||
| chr22:46155376
|
G | A | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-127+3406G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155376 | ||||||
| chr22:46155512
|
G | A | 8 | a0001c0001t0002g0039a0001c0001t0002g0185a0001c0001t0002g0189others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+3542G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155512 | ||||||
| chr22:46155607
|
G | A | 1 | a0003c0003t0010g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-127+3637G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155607 | ||||||
| chr22:46155637
|
T | G | 2 | a0001c0001t0006g0029a0001c0001t0076g0030 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+3667T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155637 | ||||||
| chr22:46155706
|
C | T | 2 | a0001c0001t0007g0120a0001c0001t0007g0121 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-127+3736C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46155706 | ||||||
| chr22:46156287
|
C | A | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-127+4317C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156287 | ||||||
| chr22:46156310
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-127+4340C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156310 | ||||||
| chr22:46156509
|
G | A | 1 | a0001c0001t0004g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-127+4539G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156509 | ||||||
| chr22:46156663
|
A | C | 46 | a0001c0001t0001g0073a0001c0001t0001g0125a0001c0001t0002g0039others(43): Show | 46 | HG01106.hp2 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.-127+4693A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156663 | ||||||
| chr22:46156824
|
A | T | 34 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(31): Show | 34 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-127+4854A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156824 | ||||||
| chr22:46156848
|
T | C | 116 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(113): Show | 116 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.-127+4878T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156848 | ||||||
| chr22:46156920
|
T | C | 40 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(37): Show | 40 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-127+4950T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156920 | ||||||
| chr22:46156983
|
C | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5013C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156983 | ||||||
| chr22:46156985
|
T | G | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5015T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156985 | ||||||
| chr22:46156987
|
C | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5017C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156987 | ||||||
| chr22:46156988
|
C | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5018C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156988 | ||||||
| chr22:46156991
|
G | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5021G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156991 | ||||||
| chr22:46156993
|
C | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5023C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156993 | ||||||
| chr22:46156997
|
G | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5027G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156997 | ||||||
| chr22:46156998
|
CCTCTTCA others(3): Show |
C | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5029_-127+503 others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46156998 | ||||||
| chr22:46157009
|
T | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5039T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157009 | ||||||
| chr22:46157009
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-127+5039T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157009 | ||||||
| chr22:46157010
|
G | GAAAAAAA others(55): Show |
1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5042_-127+504 others(66): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46157010 | |||||
| chr22:46157013
|
G | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5043G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157013 | ||||||
| chr22:46157043
|
A | T | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5073A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157043 | ||||||
| chr22:46157066
|
TCCGTCAA others(3): Show |
T | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5097_-127+510 others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157066 | ||||||
| chr22:46157091
|
C | A | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5121C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157091 | ||||||
| chr22:46157094
|
GCACCCCT others(8): Show |
G | 1 | a0001c0001t0031g0198 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-127+5125_-127+513 others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157094 | ||||||
| chr22:46157105
|
T | C | 41 | a0001c0001t0001g0073a0001c0001t0001g0125a0001c0001t0002g0039others(38): Show | 41 | HG01106.hp2 HG01109.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.-127+5135T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157105 | ||||||
| chr22:46157126
|
G | A | 75 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(72): Show | 75 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-127+5156G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157126 | ||||||
| chr22:46157339
|
T | C | 77 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(74): Show | 77 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.-127+5369T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157339 | ||||||
| chr22:46157360
|
A | C | 3 | a0001c0001t0006g0029a0001c0001t0070g0168a0001c0001t0076g0030 | 3 | HG02451.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+5390A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157360 | ||||||
| chr22:46157383
|
G | A | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-127+5413G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157383 | ||||||
| chr22:46157413
|
T | C | 101 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(98): Show | 101 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.-127+5443T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157413 | ||||||
| chr22:46157430
|
G | C | 1 | a0001c0001t0018g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-127+5460G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157430 | ||||||
| chr22:46157595
|
A | G | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-127+5625A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157595 | ||||||
| chr22:46157608
|
A | G | 33 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(30): Show | 33 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-127+5638A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157608 | ||||||
| chr22:46157755
|
C | G | 86 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(83): Show | 86 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.-127+5785C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157755 | ||||||
| chr22:46157813
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0007g0020 | 2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-127+5843G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157813 | ||||||
| chr22:46157828
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-127+5858G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157828 | ||||||
| chr22:46157923
|
A | AC | 83 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(80): Show | 83 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.-127+5953_-127+595 others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46157923 | ||||||
| chr22:46158146
|
C | T | 83 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(80): Show | 83 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.-127+6176C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46158146 | ||||||
| chr22:46158456
|
C | T | 8 | a0001c0001t0002g0039a0001c0001t0002g0185a0001c0001t0002g0189others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+6486C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46158456 | ||||||
| chr22:46158516
|
C | T | 1 | a0001c0001t0002g0166 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-127+6546C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46158516 | ||||||
| chr22:46158709
|
A | G | 2 | a0001c0001t0006g0029a0001c0001t0076g0030 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+6739A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46158709 | ||||||
| chr22:46158872
|
C | T | 8 | a0001c0001t0001g0073a0001c0001t0003g0101a0001c0001t0003g0102others(5): Show | 8 | HG01243.hp2 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+6902C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46158872 | ||||||
| chr22:46158982
|
G | A | 2 | a0001c0001t0005g0130a0001c0001t0005g0165 | 2 | HG06807.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-127+7012G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46158982 | ||||||
| chr22:46159195
|
G | GTTT | 93 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(90): Show | 93 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.-127+7227_-127+722 others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46159195 | |||||
| chr22:46159398
|
T | C | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-127+7428T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46159398 | ||||||
| chr22:46159404
|
G | C | 1 | a0001c0007t0072g0033 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-127+7434G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46159404 | ||||||
| chr22:46159411
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0009g0175 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-127+7445_-127+745 others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46159411 | |||||
| chr22:46159415
|
T | G | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-127+7445T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46159415 | ||||||
| chr22:46159416
|
T | A | 1 | a0001c0001t0002g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-127+7446T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46159416 | ||||||
| chr22:46159422
|
C | T | 49 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(46): Show | 49 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.-127+7452C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46159422 | ||||||
| chr22:46159709
|
G | A | 1 | a0004c0008t0009g0146 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-127+7739G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46159709 | ||||||
| chr22:46159872
|
G | T | 2 | a0001c0001t0006g0153a0001c0001t0026g0152 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-127+7902G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46159872 | ||||||
| chr22:46159922
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0007g0020 | 2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-127+7952G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46159922 | ||||||
| chr22:46160087
|
G | A | 1 | a0001c0001t0027g0002 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-127+8117G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160087 | ||||||
| chr22:46160090
|
T | C | 1 | a0001c0006t0032g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-127+8120T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160090 | ||||||
| chr22:46160112
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0018g0097a0001c0001t0078g0196 | 3 | HG02258.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-127+8142C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160112 | ||||||
| chr22:46160138
|
T | C | 39 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(36): Show | 39 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-127+8168T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160138 | ||||||
| chr22:46160272
|
G | A | 1 | a0001c0001t0040g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-127+8302G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160272 | ||||||
| chr22:46160467
|
G | T | 90 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(87): Show | 90 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.-127+8497G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160467 | ||||||
| chr22:46160525
|
C | T | 1 | a0001c0001t0002g0117 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-127+8555C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160525 | ||||||
| chr22:46160661
|
T | C | 9 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0006g0029others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+8691T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160661 | ||||||
| chr22:46160713
|
T | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(46): Show | 49 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.-127+8743T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160713 | ||||||
| chr22:46160725
|
T | G | 2 | a0001c0001t0006g0029a0001c0001t0076g0030 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+8755T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160725 | ||||||
| chr22:46160733
|
T | C | 2 | a0001c0001t0067g0022a0001c0001t0070g0168 | 2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-127+8763T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160733 | ||||||
| chr22:46160980
|
G | A | 5 | a0001c0001t0004g0151a0001c0001t0004g0169a0001c0001t0015g0123others(2): Show | 5 | HG01109.hp1 HG01433.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127+9010G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46160980 | ||||||
| chr22:46161262
|
A | G | 55 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-127+9292A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46161262 | ||||||
| chr22:46161370
|
A | C | 1 | a0001c0001t0035g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-127+9400A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46161370 | ||||||
| chr22:46161532
|
A | G | 10 | a0001c0001t0002g0039a0001c0001t0002g0191a0001c0001t0003g0021others(7): Show | 10 | HG01496.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-127+9562A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46161532 | ||||||
| chr22:46161555
|
C | G | 7 | a0001c0001t0016g0160a0001c0001t0027g0156a0001c0001t0029g0162others(4): Show | 7 | HG01106.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127+9585C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46161555 | ||||||
| chr22:46161717
|
C | T | 2 | a0001c0001t0006g0029a0001c0001t0076g0030 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+9747C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46161717 | ||||||
| chr22:46161772
|
T | C | 1 | a0001c0001t0035g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-127+9802T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46161772 | ||||||
| chr22:46161789
|
G | T | 33 | a0001c0001t0001g0125a0001c0001t0002g0063a0001c0001t0002g0185others(30): Show | 33 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.-127+9819G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46161789 | ||||||
| chr22:46162068
|
G | A | 5 | a0001c0001t0002g0039a0001c0001t0002g0191a0001c0001t0003g0025others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-127+10098G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162068 | ||||||
| chr22:46162070
|
A | G | 7 | a0001c0001t0016g0160a0001c0001t0027g0156a0001c0001t0029g0162others(4): Show | 7 | HG01106.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127+10100A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162070 | ||||||
| chr22:46162192
|
G | A | 5 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0012g0083others(2): Show | 5 | HG02258.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-127+10222G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162192 | ||||||
| chr22:46162266
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-127+10296C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162266 | ||||||
| chr22:46162279
|
T | C | 3 | a0001c0001t0004g0169a0001c0001t0007g0020a0001c0001t0015g0123 | 3 | HG01433.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-127+10309T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162279 | ||||||
| chr22:46162387
|
C | G | 2 | a0001c0001t0002g0039a0001c0001t0002g0191 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-127+10417C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162387 | ||||||
| chr22:46162448
|
C | T | 5 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0012g0083others(2): Show | 5 | HG02258.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-127+10478C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162448 | ||||||
| chr22:46162449
|
C | T | 1 | a0002c0002t0021g0035 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-127+10479C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162449 | ||||||
| chr22:46162490
|
G | A | 12 | a0001c0001t0001g0073a0001c0001t0003g0025a0001c0001t0003g0101others(9): Show | 12 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-127+10520G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162490 | ||||||
| chr22:46162560
|
G | A | 7 | a0001c0001t0003g0021a0001c0001t0012g0005a0001c0001t0015g0136others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127+10590G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162560 | ||||||
| chr22:46162678
|
T | C | 11 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0003g0021others(8): Show | 11 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-127+10708T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162678 | ||||||
| chr22:46162756
|
GC | G | 6 | a0001c0001t0002g0039a0001c0001t0002g0191a0001c0001t0003g0124others(3): Show | 6 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127+10788delC | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46162756 | |||||
| chr22:46162801
|
G | C | 1 | a0001c0001t0042g0105 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-127+10831G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162801 | ||||||
| chr22:46162894
|
G | C | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-127+10924G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162894 | ||||||
| chr22:46162992
|
A | G | 36 | a0001c0001t0002g0063a0001c0001t0002g0185a0001c0001t0004g0049others(33): Show | 36 | HG01106.hp2 HG01109.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.-127+11022A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46162992 | ||||||
| chr22:46163004
|
C | T | 1 | a0001c0001t0028g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-127+11034C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163004 | ||||||
| chr22:46163114
|
G | A | 37 | a0001c0001t0001g0125a0001c0001t0002g0039a0001c0001t0002g0063others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.-127+11144G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163114 | ||||||
| chr22:46163116
|
A | G | 7 | a0001c0001t0016g0160a0001c0001t0027g0156a0001c0001t0029g0162others(4): Show | 7 | HG01106.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127+11146A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163116 | ||||||
| chr22:46163116
|
A | T | 1 | a0001c0001t0054g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-127+11146A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163116 | ||||||
| chr22:46163120
|
C | G | 7 | a0001c0001t0016g0160a0001c0001t0027g0156a0001c0001t0029g0162others(4): Show | 7 | HG01106.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127+11150C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163120 | ||||||
| chr22:46163152
|
A | G | 6 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0016g0027others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127+11182A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163152 | ||||||
| chr22:46163175
|
C | G | 3 | a0001c0001t0006g0029a0001c0001t0033g0133a0001c0001t0076g0030 | 3 | HG02451.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+11205C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163175 | ||||||
| chr22:46163368
|
A | C | 122 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(119): Show | 122 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-127+11398A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163368 | ||||||
| chr22:46163575
|
G | C | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-127+11605G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163575 | ||||||
| chr22:46163738
|
G | A | 6 | a0001c0001t0003g0021a0001c0001t0004g0169a0001c0001t0018g0186others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127+11768G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163738 | ||||||
| chr22:46163944
|
G | T | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-127+11974G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46163944 | ||||||
| chr22:46164064
|
A | G | 27 | a0001c0001t0002g0063a0001c0001t0002g0185a0001c0001t0003g0025others(24): Show | 27 | HG01109.hp1 HG01943.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-127+12094A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164064 | ||||||
| chr22:46164112
|
A | G | 24 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-127+12142A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164112 | ||||||
| chr22:46164255
|
A | AT | 46 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0125others(43): Show | 46 | HG00738.hp2 HG01106.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.-127+12299dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46164255 | |||||
| chr22:46164255
|
A | ATT | 19 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(16): Show | 19 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-127+12298_-127+12 others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46164255 | |||||
| chr22:46164255
|
AT | A | 5 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0006g0106others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-127+12299delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46164255 | |||||
| chr22:46164362
|
A | C | 55 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 55 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.-126-12391A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164362 | ||||||
| chr22:46164362
|
A | T | 3 | a0001c0001t0015g0019a0001c0001t0015g0136a0001c0001t0068g0119 | 3 | HG02257.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-126-12391A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164362 | ||||||
| chr22:46164423
|
T | C | 6 | a0001c0001t0003g0021a0001c0001t0004g0169a0001c0001t0018g0186others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-12330T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164423 | ||||||
| chr22:46164514
|
A | G | 7 | a0001c0001t0001g0073a0001c0001t0003g0101a0001c0001t0003g0102others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-12239A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164514 | ||||||
| chr22:46164514
|
A | T | 1 | a0001c0001t0039g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-126-12239A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164514 | ||||||
| chr22:46164619
|
C | T | 1 | a0001c0001t0007g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-126-12134C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164619 | ||||||
| chr22:46164627
|
G | A | 22 | a0001c0001t0002g0063a0001c0001t0002g0185a0001c0001t0004g0049others(19): Show | 22 | HG01109.hp1 HG01943.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-126-12126G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164627 | ||||||
| chr22:46164868
|
C | T | 1 | a0001c0001t0023g0081 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-126-11885C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46164868 | ||||||
| chr22:46165038
|
GTTTA | G | 7 | a0001c0001t0001g0008a0001c0001t0005g0009a0001c0001t0005g0011others(4): Show | 7 | HG00738.hp2 HG01109.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-11703_-126-11 others(10): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46165038 | |||||
| chr22:46165078
|
C | T | 5 | a0001c0001t0003g0021a0001c0001t0018g0186a0001c0001t0018g0187others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-11675C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165078 | ||||||
| chr22:46165236
|
A | G | 79 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.-126-11517A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165236 | ||||||
| chr22:46165268
|
G | A | 1 | a0001c0001t0027g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-126-11485G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165268 | ||||||
| chr22:46165329
|
G | A | 1 | a0001c0001t0079g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-126-11424G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165329 | ||||||
| chr22:46165375
|
A | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-11378A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165375 | ||||||
| chr22:46165389
|
G | A | 3 | a0001c0001t0009g0175a0001c0001t0024g0180a0001c0001t0024g0181 | 3 | NA18948.hp2 NA18993.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-126-11364G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165389 | ||||||
| chr22:46165458
|
C | G | 2 | a0001c0001t0002g0195a0001c0001t0078g0196 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-126-11295C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165458 | ||||||
| chr22:46165459
|
A | T | 2 | a0001c0001t0002g0195a0001c0001t0078g0196 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-126-11294A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165459 | ||||||
| chr22:46165653
|
G | A | 37 | a0001c0001t0001g0073a0001c0001t0001g0125a0001c0001t0002g0039others(34): Show | 37 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.-126-11100G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165653 | ||||||
| chr22:46165667
|
G | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(62): Show | 65 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.-126-11086G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165667 | ||||||
| chr22:46165814
|
A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-10939A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46165814 | ||||||
| chr22:46166178
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0003g0101a0001c0001t0003g0102others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-126-10575A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166178 | ||||||
| chr22:46166187
|
T | C | 1 | a0001c0001t0057g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-126-10566T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166187 | ||||||
| chr22:46166274
|
T | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(47): Show | 50 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.-126-10479T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166274 | ||||||
| chr22:46166284
|
T | C | 53 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(50): Show | 53 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.-126-10469T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166284 | ||||||
| chr22:46166407
|
C | A | 1 | a0001c0001t0034g0158 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-126-10346C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166407 | ||||||
| chr22:46166548
|
G | T | 1 | a0001c0004t0001g0055 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-126-10205G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166548 | ||||||
| chr22:46166618
|
C | CA | 16 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(13): Show | 16 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-126-10122dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46166618 | |||||
| chr22:46166618
|
C | CAA | 34 | a0001c0001t0001g0073a0001c0001t0001g0125a0001c0001t0002g0039others(31): Show | 34 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-126-10123_-126-10 others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46166618 | |||||
| chr22:46166632
|
C | A | 19 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0101others(16): Show | 19 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-126-10121C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166632 | ||||||
| chr22:46166721
|
A | T | 1 | a0001c0001t0005g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-126-10032A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166721 | ||||||
| chr22:46166870
|
T | C | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-126-9883T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166870 | ||||||
| chr22:46166912
|
C | T | 5 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0012g0083others(2): Show | 5 | HG02258.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-9841C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166912 | ||||||
| chr22:46166957
|
G | T | 5 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0012g0083others(2): Show | 5 | HG02258.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-9796G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46166957 | ||||||
| chr22:46167060
|
A | G | 3 | a0001c0001t0015g0019a0001c0001t0015g0136a0001c0001t0068g0119 | 3 | HG02257.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-126-9693A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46167060 | ||||||
| chr22:46167234
|
A | G | 5 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0012g0083others(2): Show | 5 | HG02258.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-9519A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46167234 | ||||||
| chr22:46167425
|
T | C | 1 | a0001c0001t0038g0126 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-126-9328T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46167425 | ||||||
| chr22:46167439
|
C | G | 18 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0101others(15): Show | 18 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-126-9314C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46167439 | ||||||
| chr22:46167520
|
A | G | 6 | a0001c0001t0003g0021a0001c0001t0004g0169a0001c0001t0018g0186others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-9233A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46167520 | ||||||
| chr22:46167880
|
C | CA | 5 | a0001c0001t0002g0032a0001c0001t0011g0034a0001c0007t0072g0033others(2): Show | 5 | HG00639.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-8861dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46167880 | |||||
| chr22:46167880
|
CA | C | 44 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 44 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.-126-8861delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46167880 | |||||
| chr22:46167880
|
CAA | C | 19 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0101others(16): Show | 19 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-126-8862_-126-886 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46167880 | |||||
| chr22:46167887
|
A | T | 2 | a0001c0001t0001g0150a0001c0001t0002g0104 | 2 | NA18945.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-126-8866A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46167887 | ||||||
| chr22:46167945
|
C | T | 11 | a0001c0001t0003g0025a0001c0001t0004g0151a0001c0001t0007g0120others(8): Show | 11 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-126-8808C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46167945 | ||||||
| chr22:46167946
|
G | A | 5 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0012g0083others(2): Show | 5 | HG02258.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-8807G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46167946 | ||||||
| chr22:46168079
|
G | T | 1 | a0004c0008t0009g0146 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-126-8674G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168079 | ||||||
| chr22:46168213
|
G | A | 5 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0012g0083others(2): Show | 5 | HG02258.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-8540G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168213 | ||||||
| chr22:46168236
|
T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-8517T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168236 | ||||||
| chr22:46168284
|
G | A | 18 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0101others(15): Show | 18 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-126-8469G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168284 | ||||||
| chr22:46168328
|
G | A | 8 | a0001c0001t0001g0073a0001c0001t0003g0101a0001c0001t0003g0102others(5): Show | 8 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-8425G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168328 | ||||||
| chr22:46168331
|
A | G | 65 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(62): Show | 65 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.-126-8422A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168331 | ||||||
| chr22:46168351
|
C | CA | 42 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0071others(39): Show | 42 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-126-8375dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168351
|
C | CAA | 21 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0139others(18): Show | 21 | HG00438.hp1 HG00597.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-126-8376_-126-837 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168351
|
C | CAAAA | 8 | a0001c0001t0016g0160a0001c0001t0027g0156a0001c0001t0029g0162others(5): Show | 8 | HG01106.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-8378_-126-837 others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168351
|
C | CAAAAA | 5 | a0001c0001t0002g0039a0001c0001t0002g0191a0001c0001t0003g0124others(2): Show | 5 | HG02895.hp2 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-8379_-126-837 others(9): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168351
|
C | CAAAAAAA others(3): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-8384_-126-837 others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168351
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0009g0175a0001c0001t0010g0182a0001c0001t0046g0154 | 3 | HG03239.hp2 NA18993.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-126-8385_-126-837 others(15): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168351
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0023g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-8386_-126-837 others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168351
|
CAAA | C | 13 | a0001c0001t0001g0073a0001c0001t0003g0101a0001c0001t0003g0102others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-8377_-126-837 others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168351
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-126-8384_-126-837 others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46168351 | |||||
| chr22:46168562
|
T | C | 2 | a0001c0001t0002g0195a0001c0001t0078g0196 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-126-8191T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168562 | ||||||
| chr22:46168647
|
T | C | 1 | a0001c0001t0002g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-126-8106T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168647 | ||||||
| chr22:46168728
|
C | G | 127 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(124): Show | 127 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-126-8025C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168728 | ||||||
| chr22:46168786
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0002g0189a0001c0001t0003g0103others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-126-7967G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168786 | ||||||
| chr22:46168791
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0002g0098a0001c0001t0002g0189others(13): Show | 16 | HG00738.hp2 HG01109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-126-7962C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46168791 | ||||||
| chr22:46169017
|
A | G | 18 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0101others(15): Show | 18 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-126-7736A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169017 | ||||||
| chr22:46169121
|
T | C | 18 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0101others(15): Show | 18 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-126-7632T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169121 | ||||||
| chr22:46169153
|
C | T | 1 | a0001c0001t0007g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-126-7600C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169153 | ||||||
| chr22:46169255
|
TTTG | T | 17 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0101others(14): Show | 17 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-126-7492_-126-749 others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46169255 | |||||
| chr22:46169374
|
A | C | 23 | a0001c0001t0002g0063a0001c0001t0002g0185a0001c0001t0004g0049others(20): Show | 23 | HG01109.hp1 HG01943.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-126-7379A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169374 | ||||||
| chr22:46169379
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0002g0098a0001c0001t0002g0189others(13): Show | 16 | HG00738.hp2 HG01109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-126-7374C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169379 | ||||||
| chr22:46169391
|
C | A | 1 | a0001c0001t0025g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-126-7362C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169391 | ||||||
| chr22:46169469
|
C | T | 11 | a0001c0001t0001g0073a0001c0001t0003g0101a0001c0001t0003g0102others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-126-7284C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169469 | ||||||
| chr22:46169481
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0025g0056 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-126-7272G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169481 | ||||||
| chr22:46169626
|
C | G | 2 | a0001c0001t0006g0153a0001c0001t0026g0152 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-126-7127C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169626 | ||||||
| chr22:46169712
|
A | G | 6 | a0001c0001t0001g0171a0001c0001t0002g0032a0001c0001t0011g0034others(3): Show | 6 | HG01928.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-126-7041A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169712 | ||||||
| chr22:46169719
|
A | T | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-126-7034A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46169719 | ||||||
| chr22:46170112
|
G | GT | 13 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-6629dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170112 | |||||
| chr22:46170240
|
G | A | 2 | a0001c0001t0018g0186a0001c0001t0018g0187 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-126-6513G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46170240 | ||||||
| chr22:46170291
|
C | G | 22 | a0001c0001t0001g0008a0001c0001t0002g0098a0001c0001t0002g0189others(19): Show | 22 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.-126-6462C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46170291 | ||||||
| chr22:46170402
|
A | AT | 6 | a0001c0001t0001g0057a0001c0001t0001g0125a0001c0001t0002g0191others(3): Show | 6 | HG02071.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-6324dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170402
|
A | ATT | 15 | a0001c0001t0002g0185a0001c0001t0004g0049a0001c0001t0004g0172others(12): Show | 15 | HG01943.hp2 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-126-6325_-126-632 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170402
|
A | ATTT | 9 | a0001c0001t0002g0063a0001c0001t0004g0051a0001c0001t0006g0134others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-126-6326_-126-632 others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170402
|
AT | A | 75 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0084others(72): Show | 76 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.-126-6324delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170402
|
ATT | A | 15 | a0001c0001t0002g0039a0001c0001t0003g0124a0001c0001t0012g0083others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-126-6325_-126-632 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170402
|
ATTT | A | 6 | a0001c0001t0002g0098a0001c0001t0002g0195a0001c0001t0007g0020others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-6326_-126-632 others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170402
|
ATTTT | A | 10 | a0001c0001t0001g0008a0001c0001t0002g0189a0001c0001t0003g0103others(7): Show | 10 | HG00738.hp2 HG01109.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-126-6327_-126-632 others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170402
|
ATTTTTTT | A | 13 | a0001c0001t0001g0073a0001c0001t0003g0025a0001c0001t0003g0101others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-6330_-126-632 others(11): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170402
|
ATTTTTTT others(1): Show |
A | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-126-6331_-126-632 others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46170402 | |||||
| chr22:46170431
|
T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-6322T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46170431 | ||||||
| chr22:46170787
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0002g0191 | 2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-126-5966C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46170787 | ||||||
| chr22:46170927
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-126-5826C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46170927 | ||||||
| chr22:46171097
|
A | G | 16 | a0001c0001t0001g0073a0001c0001t0003g0025a0001c0001t0003g0101others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-126-5656A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171097 | ||||||
| chr22:46171100
|
G | A | 1 | a0001c0001t0015g0123 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-126-5653G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171100 | ||||||
| chr22:46171170
|
G | GA | 16 | a0001c0001t0001g0008a0001c0001t0002g0098a0001c0001t0002g0189others(13): Show | 16 | HG00738.hp2 HG01109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-126-5572dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46171170 | |||||
| chr22:46171223
|
G | A | 15 | a0001c0001t0002g0039a0001c0001t0003g0124a0001c0001t0006g0153others(12): Show | 15 | HG01106.hp2 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-126-5530G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171223 | ||||||
| chr22:46171311
|
T | C | 3 | a0001c0001t0015g0019a0001c0001t0015g0136a0001c0001t0068g0119 | 3 | HG02257.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-126-5442T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171311 | ||||||
| chr22:46171489
|
A | G | 46 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 46 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.-126-5264A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171489 | ||||||
| chr22:46171628
|
G | A | 1 | a0001c0001t0040g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-126-5125G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171628 | ||||||
| chr22:46171697
|
C | T | 12 | a0001c0001t0001g0073a0001c0001t0003g0025a0001c0001t0003g0101others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-126-5056C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171697 | ||||||
| chr22:46171721
|
G | A | 1 | a0001c0001t0027g0002 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-126-5032G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171721 | ||||||
| chr22:46171750
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-126-5003G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171750 | ||||||
| chr22:46171924
|
A | G | 21 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0025others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-126-4829A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171924 | ||||||
| chr22:46171959
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-126-4794G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171959 | ||||||
| chr22:46171970
|
G | A | 3 | a0001c0001t0015g0019a0001c0001t0015g0136a0001c0001t0068g0119 | 3 | HG02257.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-126-4783G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171970 | ||||||
| chr22:46171981
|
G | A | 5 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0006g0106others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-4772G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46171981 | ||||||
| chr22:46172148
|
C | A | 3 | a0001c0001t0003g0025a0001c0001t0016g0027a0001c0001t0062g0026 | 3 | HG02258.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-126-4605C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172148 | ||||||
| chr22:46172172
|
T | C | 197 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.-126-4581T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172172 | ||||||
| chr22:46172318
|
T | TA | 7 | a0001c0001t0001g0018a0001c0001t0002g0145a0001c0001t0002g0170others(4): Show | 7 | HG01516.hp1 HG02071.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-4413dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46172318 | |||||
| chr22:46172318
|
T | TAA | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0125others(9): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-126-4414_-126-441 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46172318 | |||||
| chr22:46172318
|
TA | T | 6 | a0001c0001t0002g0195a0001c0001t0004g0151a0001c0001t0013g0192others(3): Show | 6 | HG01952.hp2 HG02145.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-4413delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46172318 | |||||
| chr22:46172318
|
TAA | T | 80 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(77): Show | 80 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.-126-4414_-126-441 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46172318 | |||||
| chr22:46172318
|
TAAA | T | 5 | a0001c0001t0003g0021a0001c0001t0004g0169a0001c0001t0027g0002others(2): Show | 5 | HG01433.hp2 HG01496.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-4415_-126-441 others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46172318 | |||||
| chr22:46172331
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-126-4422A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172331 | ||||||
| chr22:46172346
|
T | C | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-126-4407T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172346 | ||||||
| chr22:46172353
|
G | T | 3 | a0001c0001t0007g0120a0001c0001t0007g0121a0001c0001t0028g0118 | 3 | HG02896.hp2 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-4400G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172353 | ||||||
| chr22:46172421
|
G | C | 20 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-126-4332G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172421 | ||||||
| chr22:46172685
|
C | T | 1 | a0001c0001t0077g0004 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-126-4068C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172685 | ||||||
| chr22:46172697
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-126-4056C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172697 | ||||||
| chr22:46172698
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-126-4055G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172698 | ||||||
| chr22:46172705
|
A | G | 7 | a0001c0001t0001g0193a0001c0001t0003g0025a0001c0001t0012g0005others(4): Show | 7 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-126-4048A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172705 | ||||||
| chr22:46172911
|
A | G | 1 | a0001c0001t0013g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-126-3842A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172911 | ||||||
| chr22:46172942
|
T | C | 11 | a0001c0001t0001g0193a0001c0001t0003g0021a0001c0001t0003g0025others(8): Show | 11 | HG01433.hp2 HG01496.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-126-3811T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46172942 | ||||||
| chr22:46173005
|
T | G | 14 | a0001c0001t0001g0073a0001c0001t0003g0101a0001c0001t0003g0102others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-126-3748T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46173005 | ||||||
| chr22:46173016
|
G | C | 1 | a0001c0001t0040g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-126-3737G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46173016 | ||||||
| chr22:46173247
|
G | A | 1 | a0001c0001t0004g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-126-3506G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46173247 | ||||||
| chr22:46173274
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0005g0007a0001c0001t0022g0067others(3): Show | 6 | HG00099.hp2 HG01106.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-3479G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46173274 | ||||||
| chr22:46173593
|
GA | G | 5 | a0001c0001t0001g0193a0001c0001t0003g0025a0001c0001t0016g0027others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-3156delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46173593 | |||||
| chr22:46173947
|
G | A | 5 | a0001c0001t0001g0193a0001c0001t0003g0025a0001c0001t0016g0027others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-2806G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46173947 | ||||||
| chr22:46174004
|
A | ACCATCCT others(18): Show |
137 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.-126-2747_-126-274 others(29): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174004 | |||||
| chr22:46174007
|
C | G | 137 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.-126-2746C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174007 | ||||||
| chr22:46174034
|
T | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2719T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174034 | ||||||
| chr22:46174041
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2712G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174041 | ||||||
| chr22:46174046
|
T | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2707T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174046 | ||||||
| chr22:46174048
|
C | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2705C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174048 | ||||||
| chr22:46174049
|
A | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2704A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174049 | ||||||
| chr22:46174052
|
T | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2701T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174052 | ||||||
| chr22:46174068
|
C | G | 1 | a0001c0001t0013g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-126-2685C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174068 | ||||||
| chr22:46174070
|
C | T | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2683C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174070 | ||||||
| chr22:46174092
|
T | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2661T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174092 | ||||||
| chr22:46174095
|
T | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2658T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174095 | ||||||
| chr22:46174103
|
A | G | 3 | a0001c0001t0006g0177a0001c0001t0012g0137a0001c0001t0076g0030 | 3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-126-2650A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174103 | ||||||
| chr22:46174110
|
A | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2643A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174110 | ||||||
| chr22:46174114
|
G | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2639G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174114 | ||||||
| chr22:46174117
|
A | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2636A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174117 | ||||||
| chr22:46174132
|
T | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2621T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174132 | ||||||
| chr22:46174133
|
G | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2620G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174133 | ||||||
| chr22:46174135
|
A | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2618A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174135 | ||||||
| chr22:46174146
|
G | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2607G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174146 | ||||||
| chr22:46174156
|
A | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2597A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174156 | ||||||
| chr22:46174164
|
A | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2589A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174164 | ||||||
| chr22:46174171
|
T | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2582T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174171 | ||||||
| chr22:46174176
|
T | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2577T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174176 | ||||||
| chr22:46174177
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2576G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174177 | ||||||
| chr22:46174181
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2572G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174181 | ||||||
| chr22:46174184
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2569G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174184 | ||||||
| chr22:46174185
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2568G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174185 | ||||||
| chr22:46174186
|
A | AAG | 8 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0005g0007others(5): Show | 8 | HG00099.hp2 HG01069.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-126-2565_-126-256 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174186 | |||||
| chr22:46174188
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2565G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174188 | ||||||
| chr22:46174188
|
GAA | G | 16 | a0001c0001t0001g0073a0001c0001t0002g0063a0001c0001t0003g0025others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-126-2563_-126-256 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174188 | |||||
| chr22:46174190
|
A | AAG | 10 | a0001c0001t0001g0138a0001c0001t0002g0032a0001c0001t0002g0108others(7): Show | 11 | HG01071.hp1 HG01169.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.-126-2536_-126-253 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174190 | |||||
| chr22:46174190
|
A | G | 8 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0005g0007others(5): Show | 8 | HG00099.hp2 HG01069.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-126-2563A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174190 | ||||||
| chr22:46174190
|
AAG | A | 56 | a0001c0001t0001g0171a0001c0001t0001g0193a0001c0001t0002g0039others(53): Show | 56 | HG00738.hp2 HG01109.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.-126-2536_-126-253 others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174190 | |||||
| chr22:46174190
|
AAGAG | A | 10 | a0001c0001t0001g0096a0001c0001t0002g0145a0001c0001t0002g0195others(7): Show | 10 | HG00438.hp2 HG01109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-126-2538_-126-253 others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174190 | |||||
| chr22:46174190
|
AAGAGAG | A | 8 | a0001c0001t0001g0125a0001c0001t0002g0191a0001c0001t0006g0029others(5): Show | 8 | HG01106.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-2540_-126-253 others(10): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174190 | |||||
| chr22:46174192
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2561G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174192 | ||||||
| chr22:46174194
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2559G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174194 | ||||||
| chr22:46174196
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2557G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174196 | ||||||
| chr22:46174198
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2555G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174198 | ||||||
| chr22:46174200
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2553G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174200 | ||||||
| chr22:46174202
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2551G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174202 | ||||||
| chr22:46174203
|
AGAGAGAG others(441): Show |
A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2549_-126-210 others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174203 | ||||||
| chr22:46174236
|
G | A | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-126-2517G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174236 | ||||||
| chr22:46174249
|
A | G | 35 | a0001c0001t0001g0125a0001c0001t0002g0039a0001c0001t0002g0191others(32): Show | 35 | HG00738.hp2 HG01106.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.-126-2504A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174249 | ||||||
| chr22:46174250
|
G | GAAGGAAG others(26): Show |
1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(37): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174250 | |||||
| chr22:46174250
|
G | GAAGGAAG others(30): Show |
1 | a0001c0001t0015g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(41): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174250 | |||||
| chr22:46174266
|
G | GAAGGAAA others(26): Show |
1 | a0001c0001t0014g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-126-2481_-126-248 others(37): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(30): Show |
22 | a0001c0001t0001g0073a0001c0001t0002g0063a0001c0001t0002g0098others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-126-2476_-126-247 others(41): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(63): Show |
2 | a0001c0001t0003g0124a0001c0001t0060g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-126-2476_-126-247 others(74): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(26): Show |
4 | a0001c0001t0004g0051a0001c0001t0004g0151a0001c0001t0061g0188others(1): Show | 4 | HG01516.hp2 HG02886.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(37): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(26): Show |
4 | a0001c0001t0008g0199a0001c0001t0016g0160a0001c0001t0020g0128others(1): Show | 4 | HG02622.hp2 HG03130.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(37): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(30): Show |
22 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0193others(19): Show | 22 | HG00099.hp2 HG01069.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(41): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(30): Show |
1 | a0001c0001t0071g0010 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(41): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(34): Show |
7 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(4): Show | 7 | HG01891.hp2 HG02071.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(45): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(34): Show |
1 | a0001c0001t0005g0011 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(45): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(38): Show |
20 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0072others(17): Show | 20 | HG00597.hp2 HG01358.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(49): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(38): Show |
5 | a0001c0001t0006g0134a0001c0001t0029g0162a0001c0001t0038g0126others(2): Show | 5 | HG02145.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(49): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(42): Show |
35 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0070others(32): Show | 36 | HG00639.hp1 HG00639.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(53): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(42): Show |
6 | a0001c0001t0001g0125a0001c0001t0002g0039a0001c0001t0002g0191others(3): Show | 6 | HG02280.hp2 HG02970.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(53): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(46): Show |
26 | a0001c0001t0001g0015a0001c0001t0001g0052a0001c0001t0001g0084others(23): Show | 26 | HG00438.hp2 HG00597.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(57): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(46): Show |
1 | a0001c0006t0026g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(57): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(50): Show |
20 | a0001c0001t0001g0150a0001c0001t0002g0104a0001c0001t0002g0145others(17): Show | 20 | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(61): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(54): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0009g0091others(4): Show | 7 | HG00099.hp1 HG01516.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(65): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(54): Show |
1 | a0001c0001t0015g0123 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(65): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(58): Show |
6 | a0001c0001t0001g0080a0001c0001t0027g0002a0001c0001t0027g0156others(3): Show | 6 | HG01496.hp2 HG02129.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-2477_-126-247 others(69): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174266
|
G | GAAGGAAG others(62): Show |
1 | a0001c0001t0034g0158 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(73): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174266 | |||||
| chr22:46174269
|
G | GGAAGGAA others(38): Show |
1 | a0001c0001t0003g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(49): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174269 | |||||
| chr22:46174269
|
G | GGAAGGAA others(58): Show |
1 | a0001c0001t0018g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-126-2477_-126-247 others(69): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174269 | |||||
| chr22:46174335
|
A | G | 110 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0068others(107): Show | 110 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(107): Show |
intron_variant | MODIFIER | c.-126-2418A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174335 | ||||||
| chr22:46174445
|
A | G | 52 | a0001c0001t0001g0015a0001c0001t0001g0073a0001c0001t0001g0125others(49): Show | 52 | HG00738.hp2 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-126-2308A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174445 | ||||||
| chr22:46174485
|
A | C | 2 | a0001c0001t0006g0143a0001c0001t0061g0188 | 2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-126-2268A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174485 | ||||||
| chr22:46174503
|
A | G | 18 | a0001c0001t0002g0195a0001c0001t0004g0037a0001c0001t0004g0051others(15): Show | 18 | HG01433.hp2 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-126-2250A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174503 | ||||||
| chr22:46174574
|
T | C | 4 | a0001c0001t0001g0096a0001c0001t0002g0104a0001c0001t0009g0091others(1): Show | 4 | HG00438.hp2 NA18952.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126-2179T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174574 | ||||||
| chr22:46174653
|
C | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-2100C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174653 | ||||||
| chr22:46174917
|
CT | C | 6 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(3): Show | 6 | HG01433.hp2 HG01891.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-1824delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46174917 | |||||
| chr22:46174933
|
A | T | 1 | a0001c0001t0037g0064 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-126-1820A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174933 | ||||||
| chr22:46174973
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-126-1780G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46174973 | ||||||
| chr22:46175056
|
C | T | 4 | a0001c0001t0002g0063a0001c0001t0002g0189a0001c0001t0012g0005others(1): Show | 4 | HG02280.hp1 HG03225.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126-1697C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175056 | ||||||
| chr22:46175059
|
G | A | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-1694G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175059 | ||||||
| chr22:46175072
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0139others(4): Show | 7 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-126-1681C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175072 | ||||||
| chr22:46175089
|
A | G | 48 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0002g0145others(45): Show | 48 | HG00099.hp2 HG01069.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.-126-1664A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175089 | ||||||
| chr22:46175317
|
T | C | 6 | a0001c0001t0001g0193a0001c0001t0002g0098a0001c0001t0002g0195others(3): Show | 6 | HG01243.hp1 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-1436T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175317 | ||||||
| chr22:46175325
|
G | C | 3 | a0001c0001t0004g0172a0001c0001t0015g0123a0001c0001t0057g0157 | 3 | HG02572.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-126-1428G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175325 | ||||||
| chr22:46175375
|
T | A | 1 | a0001c0001t0008g0109 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-126-1378T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175375 | ||||||
| chr22:46175385
|
A | G | 1 | a0001c0001t0029g0162 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-126-1368A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175385 | ||||||
| chr22:46175436
|
G | A | 1 | a0001c0001t0079g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-126-1317G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175436 | ||||||
| chr22:46175449
|
C | T | 5 | a0001c0001t0001g0193a0001c0001t0002g0098a0001c0001t0002g0195others(2): Show | 5 | HG01243.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-1304C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175449 | ||||||
| chr22:46175496
|
G | A | 4 | a0001c0001t0006g0153a0001c0001t0016g0027a0001c0001t0020g0178others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126-1257G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175496 | ||||||
| chr22:46175503
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-126-1250G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175503 | ||||||
| chr22:46175509
|
C | G | 14 | a0001c0001t0001g0017a0001c0001t0004g0037a0001c0001t0005g0009others(11): Show | 14 | HG00099.hp1 HG00738.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-126-1244C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175509 | ||||||
| chr22:46175558
|
C | T | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-126-1195C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175558 | ||||||
| chr22:46175587
|
G | A | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-126-1166G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175587 | ||||||
| chr22:46175700
|
C | T | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-126-1053C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46175700 | ||||||
| chr22:46175713
|
TA | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0148others(17): Show | 20 | HG00099.hp1 HG00738.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.-126-1024delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 46175713 | |||||
| chr22:46176044
|
T | C | 5 | a0001c0001t0001g0193a0001c0001t0002g0098a0001c0001t0002g0195others(2): Show | 5 | HG01243.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-709T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176044 | ||||||
| chr22:46176063
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0002g0166 | 2 | NA18945.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-126-690T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176063 | ||||||
| chr22:46176087
|
C | A | 13 | a0001c0001t0004g0037a0001c0001t0005g0011a0001c0001t0006g0106others(10): Show | 13 | HG00738.hp2 HG01109.hp1 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.-126-666C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176087 | ||||||
| chr22:46176097
|
C | A | 13 | a0001c0001t0003g0124a0001c0001t0006g0153a0001c0001t0016g0027others(10): Show | 13 | HG01516.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-656C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176097 | ||||||
| chr22:46176166
|
C | T | 1 | a0001c0001t0045g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-126-587C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176166 | ||||||
| chr22:46176175
|
A | T | 1 | a0001c0001t0003g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-126-578A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176175 | ||||||
| chr22:46176250
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-126-503C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176250 | ||||||
| chr22:46176260
|
C | T | 2 | a0001c0001t0004g0049a0001c0001t0066g0050 | 2 | HG01943.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-126-493C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176260 | ||||||
| chr22:46176261
|
G | A | 14 | a0001c0001t0003g0124a0001c0001t0006g0153a0001c0001t0016g0027others(11): Show | 14 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-126-492G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176261 | ||||||
| chr22:46176284
|
G | A | 13 | a0001c0001t0004g0037a0001c0001t0005g0011a0001c0001t0006g0106others(10): Show | 13 | HG00738.hp2 HG02273.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126-469G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176284 | ||||||
| chr22:46176564
|
A | G | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-126-189A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176564 | ||||||
| chr22:46176656
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-126-97C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176656 | ||||||
| chr22:46176709
|
G | A | 3 | a0001c0001t0004g0172a0001c0001t0015g0123a0001c0001t0057g0157 | 3 | HG02572.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-126-44G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 2/8 | chr22 | 46176709 | ||||||
| chr22:46176847
|
G | A | 1 | a0001c0001t0019g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-43+11G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46176847 | ||||||
| chr22:46176933
|
G | A | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-43+97G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46176933 | ||||||
| chr22:46176981
|
C | T | 1 | a0001c0001t0023g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-43+145C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46176981 | ||||||
| chr22:46176986
|
A | G | 12 | a0001c0001t0001g0125a0001c0001t0003g0147a0001c0001t0004g0172others(9): Show | 12 | HG01496.hp2 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43+150A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46176986 | ||||||
| chr22:46176997
|
T | G | 1 | a0001c0001t0008g0109 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-43+161T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46176997 | ||||||
| chr22:46176998
|
T | C | 18 | a0001c0001t0001g0193a0001c0001t0002g0063a0001c0001t0002g0098others(15): Show | 18 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.-43+162T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46176998 | ||||||
| chr22:46177006
|
T | C | 8 | a0001c0001t0002g0145a0001c0001t0004g0049a0001c0001t0008g0199others(5): Show | 8 | HG02559.hp1 HG03041.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+170T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177006 | ||||||
| chr22:46177006
|
T | G | 2 | a0001c0001t0013g0085a0001c0001t0058g0079 | 2 | HG02040.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-43+170T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177006 | ||||||
| chr22:46177008
|
A | G | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-43+172A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177008 | ||||||
| chr22:46177010
|
A | G | 1 | a0002c0002t0056g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-43+174A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177010 | ||||||
| chr22:46177021
|
T | C | 1 | a0001c0001t0002g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43+185T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177021 | ||||||
| chr22:46177022
|
A | G | 1 | a0001c0001t0013g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-43+186A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177022 | ||||||
| chr22:46177027
|
A | G | 5 | a0001c0001t0008g0199a0001c0001t0015g0136a0001c0001t0031g0198others(2): Show | 5 | HG02257.hp2 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+191A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177027 | ||||||
| chr22:46177037
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0002g0054a0001c0001t0078g0196 | 3 | HG02258.hp2 HG03130.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-43+201T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177037 | ||||||
| chr22:46177048
|
C | A | 52 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0125others(49): Show | 52 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.-43+212C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177048 | ||||||
| chr22:46177057
|
A | G | 33 | a0001c0001t0002g0185a0001c0001t0003g0101a0001c0001t0003g0102others(30): Show | 33 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.-43+221A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177057 | ||||||
| chr22:46177072
|
A | G | 6 | a0001c0001t0001g0171a0001c0001t0002g0185a0001c0001t0042g0105others(3): Show | 6 | HG01496.hp1 HG01975.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+236A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177072 | ||||||
| chr22:46177079
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-43+243C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177079 | ||||||
| chr22:46177080
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0076g0030 | 2 | NA18906.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-43+244A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177080 | ||||||
| chr22:46177143
|
A | G | 8 | a0001c0001t0005g0115a0001c0001t0007g0135a0001c0001t0014g0046others(5): Show | 8 | HG01516.hp2 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+307A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177143 | ||||||
| chr22:46177212
|
A | AAAAAT | 8 | a0001c0001t0001g0193a0001c0001t0004g0051a0001c0001t0004g0151others(5): Show | 8 | HG01516.hp2 HG02818.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43+396_-43+400dup others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46177212 | |||||
| chr22:46177296
|
A | G | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43+460A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177296 | ||||||
| chr22:46177419
|
G | A | 8 | a0001c0001t0001g0193a0001c0001t0007g0020a0001c0001t0014g0046others(5): Show | 8 | HG02622.hp1 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43+583G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177419 | ||||||
| chr22:46177463
|
CA | C | 11 | a0001c0001t0001g0073a0001c0001t0001g0193a0001c0001t0002g0098others(8): Show | 11 | HG01243.hp2 HG02622.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43+646delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46177463 | |||||
| chr22:46177463
|
CAA | C | 34 | a0001c0001t0002g0185a0001c0001t0003g0101a0001c0001t0003g0102others(31): Show | 34 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-43+645_-43+646del others(2): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46177463 | |||||
| chr22:46177755
|
G | A | 1 | a0001c0001t0035g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-43+919G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177755 | ||||||
| chr22:46177786
|
G | C | 34 | a0001c0001t0001g0193a0001c0001t0002g0185a0001c0001t0002g0195others(31): Show | 34 | HG01069.hp1 HG01109.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.-43+950G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177786 | ||||||
| chr22:46177787
|
C | T | 34 | a0001c0001t0001g0193a0001c0001t0002g0185a0001c0001t0002g0195others(31): Show | 34 | HG01069.hp1 HG01109.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.-43+951C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177787 | ||||||
| chr22:46177806
|
G | T | 6 | a0001c0001t0002g0191a0001c0001t0003g0021a0001c0001t0003g0025others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+970G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177806 | ||||||
| chr22:46177940
|
C | A | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-43+1104C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177940 | ||||||
| chr22:46177985
|
G | A | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-43+1149G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46177985 | ||||||
| chr22:46178113
|
G | A | 10 | a0001c0001t0002g0185a0001c0001t0002g0195a0001c0001t0003g0101others(7): Show | 10 | HG01433.hp2 HG01891.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43+1277G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46178113 | ||||||
| chr22:46178245
|
A | T | 1 | a0001c0001t0048g0140 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-43+1409A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46178245 | ||||||
| chr22:46178774
|
G | T | 6 | a0001c0001t0001g0125a0001c0001t0015g0136a0001c0001t0028g0118others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+1938G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46178774 | ||||||
| chr22:46179326
|
C | T | 5 | a0001c0001t0002g0098a0001c0001t0004g0172a0001c0001t0020g0178others(2): Show | 5 | HG01943.hp2 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+2490C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46179326 | ||||||
| chr22:46179461
|
G | A | 2 | a0001c0001t0003g0147a0001c0001t0018g0097 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-43+2625G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46179461 | ||||||
| chr22:46179545
|
C | T | 1 | a0001c0001t0046g0154 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-43+2709C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46179545 | ||||||
| chr22:46179722
|
C | T | 3 | a0001c0001t0006g0143a0001c0001t0026g0152a0001c0001t0039g0041 | 3 | HG01243.hp1 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43+2886C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46179722 | ||||||
| chr22:46179903
|
T | G | 1 | a0003c0003t0010g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-43+3067T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46179903 | ||||||
| chr22:46180139
|
T | C | 33 | a0001c0001t0001g0125a0001c0001t0001g0193a0001c0001t0002g0185others(30): Show | 33 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.-43+3303T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46180139 | ||||||
| chr22:46180169
|
A | G | 1 | a0001c0001t0063g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43+3333A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46180169 | ||||||
| chr22:46180194
|
C | CT | 25 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0095others(22): Show | 25 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-43+3372dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46180194 | |||||
| chr22:46180419
|
A | G | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+3583A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46180419 | ||||||
| chr22:46180575
|
A | G | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-43+3739A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46180575 | ||||||
| chr22:46180913
|
C | A | 6 | a0001c0001t0001g0125a0001c0001t0015g0136a0001c0001t0018g0186others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+4077C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46180913 | ||||||
| chr22:46180991
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0002g0185a0001c0001t0002g0195others(7): Show | 10 | HG01069.hp1 HG01433.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43+4155C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46180991 | ||||||
| chr22:46181000
|
C | T | 33 | a0001c0001t0001g0125a0001c0001t0001g0193a0001c0001t0002g0185others(30): Show | 33 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.-43+4164C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181000 | ||||||
| chr22:46181014
|
GGTGAGAG others(63): Show |
G | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-43+4206_-43+4275d others(72): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46181014 | |||||
| chr22:46181101
|
G | T | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43+4265G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181101 | ||||||
| chr22:46181214
|
G | A | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-43+4378G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181214 | ||||||
| chr22:46181226
|
C | T | 1 | a0001c0001t0014g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-43+4390C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181226 | ||||||
| chr22:46181254
|
G | A | 9 | a0001c0001t0001g0073a0001c0001t0004g0038a0001c0001t0006g0029others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43+4418G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181254 | ||||||
| chr22:46181313
|
G | T | 3 | a0001c0001t0001g0015a0001c0001t0010g0182a0001c0001t0047g0012 | 3 | HG01109.hp2 HG02293.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-43+4477G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181313 | ||||||
| chr22:46181322
|
A | G | 1 | a0001c0006t0026g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-43+4486A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181322 | ||||||
| chr22:46181583
|
A | T | 33 | a0001c0001t0001g0125a0001c0001t0001g0193a0001c0001t0002g0185others(30): Show | 33 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.-43+4747A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181583 | ||||||
| chr22:46181593
|
C | T | 13 | a0001c0001t0002g0185a0001c0001t0002g0195a0001c0001t0003g0101others(10): Show | 13 | HG01069.hp1 HG01433.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43+4757C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181593 | ||||||
| chr22:46181614
|
G | T | 30 | a0001c0001t0001g0125a0001c0001t0001g0193a0001c0001t0002g0185others(27): Show | 30 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.-43+4778G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181614 | ||||||
| chr22:46181642
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-43+4806C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46181642 | ||||||
| chr22:46182047
|
C | G | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+5211C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46182047 | ||||||
| chr22:46182056
|
G | A | 1 | a0001c0001t0005g0011 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-43+5220G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46182056 | ||||||
| chr22:46182422
|
G | A | 5 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+5586G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46182422 | ||||||
| chr22:46182613
|
G | A | 6 | a0001c0001t0009g0173a0001c0001t0009g0175a0001c0001t0024g0180others(3): Show | 6 | HG00438.hp1 HG02071.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+5777G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46182613 | ||||||
| chr22:46182657
|
G | A | 3 | a0001c0001t0015g0123a0001c0001t0041g0190a0001c0001t0057g0157 | 3 | HG02055.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-43+5821G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46182657 | ||||||
| chr22:46183150
|
A | G | 1 | a0001c0001t0063g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43+6314A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183150 | ||||||
| chr22:46183224
|
G | A | 1 | a0001c0001t0013g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-43+6388G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183224 | ||||||
| chr22:46183338
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+6502C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183338 | ||||||
| chr22:46183468
|
T | G | 30 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0095others(27): Show | 30 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-43+6632T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183468 | ||||||
| chr22:46183513
|
G | C | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+6677G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183513 | ||||||
| chr22:46183569
|
C | T | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-43+6733C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183569 | ||||||
| chr22:46183578
|
C | T | 2 | a0001c0001t0007g0020a0001c0001t0014g0046 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-43+6742C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183578 | ||||||
| chr22:46183592
|
A | G | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-43+6756A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183592 | ||||||
| chr22:46183635
|
G | A | 10 | a0001c0001t0002g0185a0001c0001t0002g0195a0001c0001t0003g0101others(7): Show | 10 | HG01433.hp2 HG01891.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43+6799G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183635 | ||||||
| chr22:46183663
|
G | C | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+6827G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183663 | ||||||
| chr22:46183703
|
T | C | 56 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0095others(53): Show | 56 | HG00597.hp1 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.-43+6867T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183703 | ||||||
| chr22:46183740
|
CCAAAACA others(3): Show |
C | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-43+6920_-43+6929d others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46183740 | |||||
| chr22:46183800
|
G | T | 4 | a0001c0001t0006g0153a0001c0001t0015g0123a0001c0001t0016g0027others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+6964G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46183800 | ||||||
| chr22:46184114
|
A | C | 5 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+7278A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184114 | ||||||
| chr22:46184144
|
A | G | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+7308A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184144 | ||||||
| chr22:46184250
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0007g0036 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-43+7414C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184250 | ||||||
| chr22:46184268
|
G | T | 1 | a0001c0006t0032g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-43+7432G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184268 | ||||||
| chr22:46184408
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-43+7572T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184408 | ||||||
| chr22:46184531
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-43+7695T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184531 | ||||||
| chr22:46184533
|
T | C | 5 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+7697T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184533 | ||||||
| chr22:46184564
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-43+7728C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184564 | ||||||
| chr22:46184645
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-43+7809G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184645 | ||||||
| chr22:46184696
|
A | G | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+7860A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184696 | ||||||
| chr22:46184757
|
A | T | 1 | a0001c0001t0038g0126 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-43+7921A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184757 | ||||||
| chr22:46184833
|
C | T | 2 | a0001c0001t0028g0118a0001c0001t0079g0107 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-43+7997C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184833 | ||||||
| chr22:46184893
|
C | T | 3 | a0001c0001t0015g0123a0001c0001t0020g0178a0001c0001t0057g0157 | 3 | HG02572.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-43+8057C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184893 | ||||||
| chr22:46184926
|
G | A | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+8090G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46184926 | ||||||
| chr22:46185026
|
A | G | 22 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0122others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-43+8190A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185026 | ||||||
| chr22:46185172
|
T | C | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+8336T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185172 | ||||||
| chr22:46185194
|
A | G | 5 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+8358A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185194 | ||||||
| chr22:46185261
|
A | G | 1 | a0001c0001t0015g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-43+8425A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185261 | ||||||
| chr22:46185478
|
T | C | 2 | a0001c0001t0006g0134a0001c0001t0006g0197 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-43+8642T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185478 | ||||||
| chr22:46185608
|
C | T | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+8772C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185608 | ||||||
| chr22:46185711
|
A | G | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-43+8875A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185711 | ||||||
| chr22:46185787
|
C | T | 4 | a0001c0001t0006g0153a0001c0001t0015g0123a0001c0001t0020g0178others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+8951C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185787 | ||||||
| chr22:46185788
|
G | A | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+8952G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185788 | ||||||
| chr22:46185820
|
A | G | 5 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+8984A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185820 | ||||||
| chr22:46185894
|
C | CAAA | 2 | a0001c0001t0001g0125a0001c0001t0006g0153 | 2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+9058_-43+9059i others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185894 | ||||||
| chr22:46185894
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0014g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-43+9058_-43+9059i others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185894 | ||||||
| chr22:46185894
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0122a0001c0001t0013g0192a0001c0001t0051g0024 | 3 | HG01167.hp2 HG02273.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.-43+9058_-43+9059i others(13): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185894 | ||||||
| chr22:46185894
|
C | CAAAAAAA others(5): Show |
10 | a0001c0001t0011g0034a0001c0001t0011g0094a0001c0001t0013g0085others(7): Show | 10 | HG01884.hp2 HG01928.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43+9058_-43+9059i others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185894 | ||||||
| chr22:46185894
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0003g0124a0001c0001t0060g0129a0001c0001t0061g0188others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43+9058_-43+9059i others(15): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185894 | ||||||
| chr22:46185894
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0095a0002c0002t0043g0111 | 2 | HG01943.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-43+9058_-43+9059i others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185894 | ||||||
| chr22:46185895
|
C | A | 49 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0122others(46): Show | 49 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.-43+9059C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185895 | ||||||
| chr22:46185895
|
C | CAA | 6 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0090others(3): Show | 6 | HG01978.hp1 HG02040.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+9080_-43+9081d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185895 | |||||
| chr22:46185895
|
CA | C | 7 | a0001c0001t0002g0189a0001c0001t0004g0038a0001c0001t0005g0028others(4): Show | 7 | HG01069.hp1 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43+9081delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185895 | |||||
| chr22:46185895
|
CAA | C | 5 | a0001c0001t0005g0011a0001c0001t0006g0134a0001c0001t0028g0127others(2): Show | 5 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+9080_-43+9081d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185895 | |||||
| chr22:46185895
|
CAAA | C | 6 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(3): Show | 6 | HG01891.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+9079_-43+9081d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185895 | |||||
| chr22:46185908
|
AAAAAAAA others(29): Show |
A | 3 | a0001c0001t0004g0049a0001c0001t0004g0060a0001c0001t0012g0083 | 3 | HG02559.hp1 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-43+9074_-43+9109d others(38): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185908 | |||||
| chr22:46185910
|
A | ATAT | 2 | a0001c0001t0002g0098a0001c0006t0032g0132 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-43+9074_-43+9075i others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185910 | ||||||
| chr22:46185910
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-43+9076_-43+9087d others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185910 | |||||
| chr22:46185910
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0005g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-43+9076_-43+9089d others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185910 | |||||
| chr22:46185912
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0065g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-43+9076_-43+9077i others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185912 | ||||||
| chr22:46185912
|
A | T | 3 | a0001c0001t0002g0098a0001c0001t0005g0115a0001c0006t0032g0132 | 3 | HG03139.hp2 HG03225.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-43+9076A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185912 | ||||||
| chr22:46185912
|
AAAAAATA others(3): Show |
A | 1 | a0001c0001t0045g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-43+9078_-43+9087d others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185912 | |||||
| chr22:46185913
|
AAAAATAT others(4): Show |
A | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-43+9079_-43+9089d others(13): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185913 | |||||
| chr22:46185913
|
AAAAATAT others(6): Show |
A | 1 | a0001c0001t0064g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-43+9079_-43+9091d others(15): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185913 | |||||
| chr22:46185913
|
AAAAATAT others(8): Show |
A | 1 | a0001c0001t0027g0002 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-43+9079_-43+9093d others(17): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185913 | |||||
| chr22:46185914
|
A | ATAT | 3 | a0001c0001t0001g0193a0001c0001t0029g0162a0001c0001t0033g0133 | 3 | HG02145.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-43+9078_-43+9079i others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185914 | ||||||
| chr22:46185914
|
A | T | 5 | a0001c0001t0002g0098a0001c0001t0005g0011a0001c0001t0005g0115others(2): Show | 5 | HG00738.hp2 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+9078A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185914 | ||||||
| chr22:46185914
|
AAAATATA others(3): Show |
A | 1 | a0001c0001t0006g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-43+9080_-43+9089d others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185914 | |||||
| chr22:46185914
|
AAAATATA others(15): Show |
A | 4 | a0001c0001t0004g0051a0001c0001t0004g0151a0001c0001t0004g0172others(1): Show | 4 | HG01943.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+9080_-43+9101d others(24): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185914 | |||||
| chr22:46185915
|
AAATATAT others(8): Show |
A | 1 | a0001c0001t0027g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-43+9081_-43+9095d others(17): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185915 | |||||
| chr22:46185915
|
AAATATAT others(10): Show |
A | 1 | a0001c0001t0040g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-43+9081_-43+9097d others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185915 | |||||
| chr22:46185915
|
AAATATAT others(18): Show |
A | 1 | a0001c0001t0001g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-43+9081_-43+9105d others(27): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185915 | |||||
| chr22:46185916
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0004g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-43+9081_-43+9082i others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185916 | |||||
| chr22:46185916
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-43+9081_-43+9082i others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185916 | |||||
| chr22:46185916
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0069g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-43+9081_-43+9082i others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185916 | |||||
| chr22:46185916
|
A | AAT | 7 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0071others(4): Show | 7 | HG00597.hp2 HG01516.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+9128_-43+9129d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185916 | |||||
| chr22:46185916
|
A | T | 31 | a0001c0001t0001g0150a0001c0001t0001g0193a0001c0001t0002g0098others(28): Show | 31 | HG00738.hp2 HG01891.hp2 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-43+9080A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185916 | ||||||
| chr22:46185916
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0018g0186a0001c0001t0028g0118a0001c0006t0026g0142 | 3 | HG01167.hp1 HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-43+9120_-43+9129d others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185916 | |||||
| chr22:46185917
|
AT | A | 2 | a0001c0001t0019g0088a0001c0001t0049g0092 | 2 | HG01358.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-43+9082delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185917 | ||||||
| chr22:46185917
|
ATAT | A | 3 | a0001c0001t0005g0009a0001c0001t0055g0155a0001c0001t0077g0004 | 3 | HG02165.hp2 HG02683.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-43+9082_-43+9084d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185917 | ||||||
| chr22:46185917
|
ATATAT | A | 2 | a0001c0001t0001g0096a0001c0001t0075g0006 | 2 | HG00438.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-43+9082_-43+9086d others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185917 | ||||||
| chr22:46185917
|
ATATATAT | A | 2 | a0001c0001t0020g0128a0001c0001t0041g0190 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-43+9082_-43+9088d others(9): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185917 | ||||||
| chr22:46185917
|
ATATATAT others(4): Show |
A | 3 | a0001c0001t0001g0148a0001c0001t0018g0187a0001c0001t0073g0042 | 3 | HG01169.hp2 HG03540.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-43+9082_-43+9092d others(13): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185917 | ||||||
| chr22:46185917
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0004g0169a0001c0001t0035g0163 | 2 | HG01433.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-43+9082_-43+9094d others(15): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185917 | ||||||
| chr22:46185917
|
ATATATAT others(10): Show |
A | 2 | a0001c0001t0002g0195a0001c0001t0079g0107 | 2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-43+9082_-43+9098d others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185917 | ||||||
| chr22:46185917
|
ATATATAT others(16): Show |
A | 3 | a0001c0001t0006g0143a0001c0001t0026g0152a0001c0001t0039g0041 | 3 | HG01243.hp1 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43+9082_-43+9104d others(25): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185917 | ||||||
| chr22:46185918
|
T | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0070others(38): Show | 42 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-43+9082T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185918 | ||||||
| chr22:46185920
|
T | A | 27 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0122others(24): Show | 28 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-43+9084T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185920 | ||||||
| chr22:46185920
|
T | C | 1 | a0001c0001t0010g0040 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-43+9084T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185920 | ||||||
| chr22:46185922
|
T | A | 21 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0122others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.-43+9086T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185922 | ||||||
| chr22:46185924
|
T | A | 18 | a0001c0001t0001g0080a0001c0001t0001g0096a0001c0001t0005g0009others(15): Show | 18 | HG00438.hp2 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-43+9088T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185924 | ||||||
| chr22:46185926
|
T | A | 7 | a0001c0001t0001g0096a0001c0001t0005g0009a0001c0001t0007g0036others(4): Show | 7 | HG00438.hp2 HG02055.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+9090T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185926 | ||||||
| chr22:46185928
|
T | A | 8 | a0001c0001t0001g0096a0001c0001t0005g0009a0001c0001t0007g0036others(5): Show | 8 | HG00438.hp2 HG01167.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+9092T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185928 | ||||||
| chr22:46185930
|
T | A | 8 | a0001c0001t0001g0148a0001c0001t0005g0009a0001c0001t0007g0036others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+9094T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185930 | ||||||
| chr22:46185932
|
T | A | 5 | a0001c0001t0001g0148a0001c0001t0004g0169a0001c0001t0005g0009others(2): Show | 5 | HG01433.hp2 HG02055.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+9096T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185932 | ||||||
| chr22:46185932
|
TATATATA others(27): Show |
T | 2 | a0001c0001t0025g0058a0001c0001t0050g0078 | 2 | HG02523.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-43+9098_-43+9131d others(36): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185932 | |||||
| chr22:46185934
|
T | A | 4 | a0001c0001t0001g0148a0001c0001t0004g0169a0001c0001t0005g0009others(1): Show | 4 | HG01433.hp2 HG02683.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+9098T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185934 | ||||||
| chr22:46185936
|
T | A | 3 | a0001c0001t0004g0169a0001c0001t0005g0009a0001c0001t0079g0107 | 3 | HG01433.hp2 HG02683.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-43+9100T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185936 | ||||||
| chr22:46185936
|
T | C | 1 | a0001c0001t0015g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-43+9100T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185936 | ||||||
| chr22:46185938
|
T | A | 3 | a0001c0001t0004g0169a0001c0001t0005g0009a0001c0001t0079g0107 | 3 | HG01433.hp2 HG02683.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-43+9102T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185938 | ||||||
| chr22:46185938
|
T | C | 1 | a0001c0001t0015g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-43+9102T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185938 | ||||||
| chr22:46185938
|
TATATATA others(21): Show |
T | 2 | a0001c0001t0009g0091a0003c0003t0010g0031 | 2 | HG04184.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-43+9104_-43+9131d others(30): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185938 | |||||
| chr22:46185940
|
T | A | 1 | a0001c0001t0004g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-43+9104T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185940 | ||||||
| chr22:46185940
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+9104T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185940 | ||||||
| chr22:46185942
|
T | A | 1 | a0001c0001t0004g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-43+9106T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185942 | ||||||
| chr22:46185942
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+9106T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185942 | ||||||
| chr22:46185942
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0002g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-43+9108_-43+9131d others(26): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185942 | |||||
| chr22:46185944
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+9108T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185944 | ||||||
| chr22:46185944
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0001g0110a0004c0008t0009g0146 | 2 | HG02698.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-43+9110_-43+9131d others(24): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185944 | |||||
| chr22:46185946
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+9110T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185946 | ||||||
| chr22:46185946
|
TATATATA others(13): Show |
T | 2 | a0001c0001t0001g0171a0001c0001t0042g0105 | 2 | HG01496.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-43+9112_-43+9131d others(22): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185946 | |||||
| chr22:46185948
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+9112T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185948 | ||||||
| chr22:46185950
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+9114T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185950 | ||||||
| chr22:46185950
|
TATATATA others(9): Show |
T | 3 | a0001c0001t0001g0084a0001c0001t0001g0184a0001c0001t0008g0167 | 3 | HG02109.hp2 HG03239.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-43+9116_-43+9131d others(18): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185950 | |||||
| chr22:46185952
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-43+9116T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185952 | ||||||
| chr22:46185952
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0025g0056a0001c0001t0058g0079 | 2 | HG02523.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-43+9118_-43+9131d others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185952 | |||||
| chr22:46185954
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0015g0136a0001c0001t0070g0168 | 3 | HG02257.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-43+9118T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185954 | ||||||
| chr22:46185954
|
TATATATA others(5): Show |
T | 2 | a0001c0001t0007g0036a0001c0001t0074g0112 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-43+9120_-43+9131d others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185954 | |||||
| chr22:46185956
|
T | C | 10 | a0001c0001t0001g0125a0001c0001t0006g0153a0001c0001t0015g0123others(7): Show | 10 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43+9120T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185956 | ||||||
| chr22:46185958
|
T | C | 9 | a0001c0001t0001g0125a0001c0001t0006g0153a0001c0001t0015g0123others(6): Show | 9 | HG02055.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43+9122T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185958 | ||||||
| chr22:46185958
|
TATATATA others(1): Show |
T | 4 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0087others(1): Show | 4 | HG00099.hp1 HG00639.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+9124_-43+9131d others(10): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185958 | |||||
| chr22:46185960
|
T | C | 36 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0122others(33): Show | 36 | HG01069.hp2 HG01071.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.-43+9124T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185960 | ||||||
| chr22:46185962
|
T | C | 36 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0122others(33): Show | 36 | HG01069.hp2 HG01071.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.-43+9126T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185962 | ||||||
| chr22:46185962
|
T | TACAC | 2 | a0001c0001t0014g0077a0001c0001t0051g0024 | 2 | HG01167.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-43+9127_-43+9128i others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185962 | |||||
| chr22:46185962
|
TATAC | T | 3 | a0001c0001t0002g0054a0001c0001t0030g0001a0001c0001t0052g0066 | 4 | HG01071.hp1 HG01169.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+9128_-43+9131d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185962 | |||||
| chr22:46185964
|
T | C | 49 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0122others(46): Show | 49 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-43+9128T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185964 | ||||||
| chr22:46185964
|
T | TACACAC | 7 | a0001c0001t0003g0124a0001c0001t0008g0199a0001c0001t0014g0048others(4): Show | 7 | HG02886.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+9133_-43+9138d others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185964 | |||||
| chr22:46185964
|
TAC | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0065a0001c0001t0022g0067others(1): Show | 4 | HG00639.hp2 HG01952.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+9137_-43+9138d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46185964 | |||||
| chr22:46185966
|
C | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-43+9130C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185966 | ||||||
| chr22:46185968
|
C | T | 3 | a0001c0001t0016g0160a0001c0001t0016g0194a0001c0001t0065g0047 | 3 | HG02486.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-43+9132C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46185968 | ||||||
| chr22:46186091
|
G | A | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+9255G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186091 | ||||||
| chr22:46186175
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-43+9339T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186175 | ||||||
| chr22:46186196
|
C | A | 2 | a0001c0001t0001g0110a0001c0001t0002g0054 | 2 | HG02698.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-43+9360C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186196 | ||||||
| chr22:46186332
|
G | A | 12 | a0001c0001t0002g0185a0001c0001t0002g0195a0001c0001t0003g0124others(9): Show | 12 | HG01496.hp2 HG02886.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43+9496G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186332 | ||||||
| chr22:46186346
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-43+9510A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186346 | ||||||
| chr22:46186382
|
G | A | 2 | a0001c0001t0007g0120a0001c0001t0007g0121 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-43+9546G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186382 | ||||||
| chr22:46186476
|
G | C | 2 | a0001c0001t0007g0020a0001c0001t0014g0046 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-43+9640G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186476 | ||||||
| chr22:46186609
|
G | C | 1 | a0001c0001t0003g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-43+9773G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186609 | ||||||
| chr22:46186670
|
G | A | 3 | a0001c0001t0058g0079a0001c0001t0073g0042a0001c0001t0074g0112 | 3 | HG02895.hp1 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-43+9834G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186670 | ||||||
| chr22:46186694
|
G | C | 5 | a0001c0001t0006g0143a0001c0001t0017g0100a0001c0001t0026g0152others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+9858G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186694 | ||||||
| chr22:46186702
|
G | A | 12 | a0001c0001t0002g0185a0001c0001t0002g0195a0001c0001t0003g0124others(9): Show | 12 | HG01496.hp2 HG02886.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43+9866G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186702 | ||||||
| chr22:46186844
|
G | A | 13 | a0001c0001t0001g0125a0001c0001t0005g0009a0001c0001t0006g0153others(10): Show | 13 | HG01167.hp2 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43+10008G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186844 | ||||||
| chr22:46186941
|
G | A | 13 | a0001c0001t0001g0125a0001c0001t0005g0009a0001c0001t0006g0153others(10): Show | 13 | HG01167.hp2 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43+10105G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46186941 | ||||||
| chr22:46187094
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0093a0001c0001t0009g0091others(1): Show | 4 | HG02040.hp1 HG02071.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+10258C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46187094 | ||||||
| chr22:46187242
|
A | T | 2 | a0001c0001t0018g0186a0001c0001t0018g0187 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-43+10406A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46187242 | ||||||
| chr22:46187636
|
T | C | 2 | a0001c0001t0004g0169a0001c0001t0007g0036 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-42-10706T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46187636 | ||||||
| chr22:46187639
|
A | G | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-42-10703A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46187639 | ||||||
| chr22:46187885
|
C | T | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-10457C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46187885 | ||||||
| chr22:46188071
|
C | G | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-42-10271C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188071 | ||||||
| chr22:46188078
|
C | A | 4 | a0001c0001t0009g0175a0001c0001t0024g0180a0001c0001t0024g0181others(1): Show | 4 | NA18948.hp2 NA18993.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-10264C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188078 | ||||||
| chr22:46188402
|
C | A | 10 | a0001c0001t0005g0009a0001c0001t0007g0120a0001c0001t0007g0121others(7): Show | 10 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42-9940C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188402 | ||||||
| chr22:46188473
|
C | G | 2 | a0001c0001t0005g0009a0001c0001t0051g0024 | 2 | HG01167.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-42-9869C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188473 | ||||||
| chr22:46188475
|
AG | A | 5 | a0001c0001t0006g0106a0001c0001t0006g0134a0001c0001t0006g0177others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-9866delG | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188475 | ||||||
| chr22:46188492
|
T | C | 197 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.-42-9850T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188492 | ||||||
| chr22:46188531
|
C | A | 1 | a0001c0001t0002g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-42-9811C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188531 | ||||||
| chr22:46188621
|
G | A | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-42-9721G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188621 | ||||||
| chr22:46188661
|
G | A | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-42-9681G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46188661 | ||||||
| chr22:46189087
|
A | G | 39 | a0001c0001t0001g0125a0001c0001t0002g0185a0001c0001t0002g0195others(36): Show | 39 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.-42-9255A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189087 | ||||||
| chr22:46189182
|
C | T | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-42-9160C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189182 | ||||||
| chr22:46189224
|
A | T | 1 | a0001c0001t0023g0081 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-42-9118A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189224 | ||||||
| chr22:46189319
|
G | A | 3 | a0001c0001t0006g0143a0001c0001t0026g0152a0001c0001t0039g0041 | 3 | HG01243.hp1 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-42-9023G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189319 | ||||||
| chr22:46189531
|
C | T | 20 | a0001c0001t0001g0125a0001c0001t0002g0185a0001c0001t0002g0195others(17): Show | 20 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-42-8811C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189531 | ||||||
| chr22:46189543
|
T | C | 40 | a0001c0001t0001g0125a0001c0001t0002g0185a0001c0001t0002g0195others(37): Show | 40 | HG00738.hp2 HG01069.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.-42-8799T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189543 | ||||||
| chr22:46189712
|
C | CT | 11 | a0001c0001t0001g0073a0001c0001t0004g0038a0001c0001t0005g0009others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-42-8618dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46189712 | |||||
| chr22:46189739
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-42-8603C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189739 | ||||||
| chr22:46189792
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-42-8550G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189792 | ||||||
| chr22:46189855
|
T | C | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-8487T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189855 | ||||||
| chr22:46189864
|
G | A | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-8478G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189864 | ||||||
| chr22:46189975
|
G | T | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-8367G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46189975 | ||||||
| chr22:46190004
|
C | T | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-8338C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190004 | ||||||
| chr22:46190097
|
C | T | 5 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42-8245C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190097 | ||||||
| chr22:46190213
|
G | A | 34 | a0001c0001t0001g0125a0001c0001t0002g0185a0001c0001t0002g0195others(31): Show | 34 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-42-8129G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190213 | ||||||
| chr22:46190361
|
T | G | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-42-7981T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190361 | ||||||
| chr22:46190389
|
A | G | 1 | a0001c0001t0020g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-42-7953A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190389 | ||||||
| chr22:46190426
|
G | A | 1 | a0001c0001t0015g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-42-7916G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190426 | ||||||
| chr22:46190430
|
G | A | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-42-7912G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190430 | ||||||
| chr22:46190691
|
G | A | 5 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42-7651G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190691 | ||||||
| chr22:46190856
|
G | C | 1 | a0001c0001t0057g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-42-7486G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190856 | ||||||
| chr22:46190942
|
G | C | 1 | a0001c0001t0018g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-42-7400G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190942 | ||||||
| chr22:46190966
|
G | A | 2 | a0001c0001t0027g0002a0001c0001t0027g0156 | 2 | HG01496.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-42-7376G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190966 | ||||||
| chr22:46190989
|
A | C | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-42-7353A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46190989 | ||||||
| chr22:46191050
|
G | A | 1 | a0003c0003t0059g0045 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-42-7292G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191050 | ||||||
| chr22:46191054
|
G | A | 4 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0060g0129others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42-7288G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191054 | ||||||
| chr22:46191084
|
T | C | 26 | a0001c0001t0001g0125a0001c0001t0002g0185a0001c0001t0002g0195others(23): Show | 26 | HG00738.hp2 HG01069.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.-42-7258T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191084 | ||||||
| chr22:46191125
|
G | A | 2 | a0001c0001t0017g0100a0001c0001t0068g0119 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42-7217G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191125 | ||||||
| chr22:46191192
|
T | G | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-42-7150T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191192 | ||||||
| chr22:46191405
|
G | A | 1 | a0001c0001t0046g0154 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-42-6937G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191405 | ||||||
| chr22:46191485
|
G | GT | 11 | a0001c0001t0001g0184a0001c0001t0002g0075a0001c0001t0002g0195others(8): Show | 11 | HG00597.hp2 HG01516.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-42-6841dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46191485 | |||||
| chr22:46191485
|
GT | G | 9 | a0001c0001t0001g0193a0001c0001t0002g0185a0001c0001t0003g0101others(6): Show | 9 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42-6841delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46191485 | |||||
| chr22:46191485
|
GTT | G | 6 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42-6842_-42-6841d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46191485 | |||||
| chr22:46191489
|
T | G | 11 | a0001c0001t0001g0125a0001c0001t0003g0147a0001c0001t0006g0153others(8): Show | 11 | HG02257.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-42-6853T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191489 | ||||||
| chr22:46191490
|
T | G | 1 | a0001c0001t0016g0027 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-42-6852T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191490 | ||||||
| chr22:46191628
|
G | A | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-42-6714G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191628 | ||||||
| chr22:46191699
|
A | G | 1 | a0001c0004t0001g0055 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-42-6643A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191699 | ||||||
| chr22:46191856
|
A | T | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-42-6486A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191856 | ||||||
| chr22:46191891
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-42-6451C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46191891 | ||||||
| chr22:46192006
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-42-6336G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46192006 | ||||||
| chr22:46192013
|
C | T | 2 | a0001c0001t0041g0190a0001c0001t0066g0050 | 2 | HG01943.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-42-6329C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46192013 | ||||||
| chr22:46192023
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-42-6319C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46192023 | ||||||
| chr22:46192381
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0070 | 2 | HG00099.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-42-5961C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46192381 | ||||||
| chr22:46192441
|
G | A | 4 | a0001c0001t0004g0169a0001c0001t0007g0036a0001c0001t0073g0042others(1): Show | 4 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42-5901G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46192441 | ||||||
| chr22:46192531
|
T | A | 1 | a0001c0001t0018g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-42-5811T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46192531 | ||||||
| chr22:46193074
|
G | T | 1 | a0001c0001t0055g0155 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-42-5268G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193074 | ||||||
| chr22:46193208
|
G | A | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-5134G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193208 | ||||||
| chr22:46193215
|
C | T | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-42-5127C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193215 | ||||||
| chr22:46193216
|
G | A | 2 | a0001c0001t0008g0199a0001c0001t0031g0198 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-42-5126G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193216 | ||||||
| chr22:46193248
|
G | C | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-5094G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193248 | ||||||
| chr22:46193318
|
T | C | 1 | a0001c0001t0002g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-42-5024T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193318 | ||||||
| chr22:46193346
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-42-4996G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193346 | ||||||
| chr22:46193380
|
T | C | 3 | a0001c0001t0004g0038a0001c0001t0006g0029a0001c0001t0033g0133 | 3 | HG02451.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42-4962T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193380 | ||||||
| chr22:46193433
|
A | G | 7 | a0001c0001t0006g0153a0001c0001t0007g0020a0001c0001t0014g0046others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42-4909A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193433 | ||||||
| chr22:46193664
|
G | T | 11 | a0001c0001t0002g0185a0001c0001t0002g0195a0001c0001t0003g0124others(8): Show | 11 | HG01496.hp2 HG02886.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-42-4678G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193664 | ||||||
| chr22:46193753
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-42-4589C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193753 | ||||||
| chr22:46193802
|
T | G | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-42-4540T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193802 | ||||||
| chr22:46193899
|
C | G | 1 | a0001c0001t0003g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-42-4443C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46193899 | ||||||
| chr22:46194154
|
C | T | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-42-4188C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46194154 | ||||||
| chr22:46194374
|
C | T | 1 | a0001c0001t0023g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-42-3968C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46194374 | ||||||
| chr22:46194381
|
A | G | 40 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(37): Show | 40 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.-42-3961A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46194381 | ||||||
| chr22:46194415
|
C | T | 4 | a0001c0001t0018g0186a0001c0001t0018g0187a0001c0001t0028g0118others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-3927C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46194415 | ||||||
| chr22:46194568
|
C | CT | 16 | a0001c0001t0001g0018a0001c0001t0001g0138a0001c0001t0002g0039others(13): Show | 16 | HG01516.hp1 HG01943.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-42-3753dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46194568 | |||||
| chr22:46194568
|
CT | C | 56 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(53): Show | 56 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.-42-3753delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46194568 | |||||
| chr22:46194589
|
T | G | 22 | a0001c0001t0002g0185a0001c0001t0002g0191a0001c0001t0002g0195others(19): Show | 22 | HG01496.hp2 HG02572.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.-42-3753T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46194589 | ||||||
| chr22:46194592
|
G | C | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-42-3750G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46194592 | ||||||
| chr22:46194893
|
CT | C | 31 | a0001c0001t0001g0073a0001c0001t0001g0193a0001c0001t0002g0166others(28): Show | 31 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.-42-3431delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46194893 | |||||
| chr22:46194893
|
CTT | C | 8 | a0001c0001t0006g0153a0001c0001t0012g0137a0001c0001t0014g0046others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-3432_-42-3431d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46194893 | |||||
| chr22:46194897
|
T | C | 32 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(29): Show | 32 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.-42-3445T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46194897 | ||||||
| chr22:46194898
|
T | C | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-3444T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46194898 | ||||||
| chr22:46195047
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0007g0036 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-42-3295C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195047 | ||||||
| chr22:46195231
|
C | A | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-42-3111C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195231 | ||||||
| chr22:46195469
|
C | CTT | 48 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0193others(45): Show | 48 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-42-2872_-42-2871d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46195469 | |||||
| chr22:46195657
|
A | G | 20 | a0001c0001t0002g0185a0001c0001t0002g0195a0001c0001t0003g0124others(17): Show | 20 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-42-2685A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195657 | ||||||
| chr22:46195738
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-42-2604T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195738 | ||||||
| chr22:46195787
|
G | C | 5 | a0001c0001t0001g0193a0001c0001t0018g0186a0001c0001t0018g0187others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-2555G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195787 | ||||||
| chr22:46195805
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0007g0036 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-42-2537C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195805 | ||||||
| chr22:46195828
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0009a0001c0001t0022g0076others(3): Show | 6 | HG00639.hp1 HG01167.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42-2514G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195828 | ||||||
| chr22:46195855
|
A | G | 48 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0193others(45): Show | 48 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-42-2487A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195855 | ||||||
| chr22:46195885
|
C | T | 1 | a0001c0001t0016g0027 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-42-2457C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195885 | ||||||
| chr22:46195894
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-42-2448C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195894 | ||||||
| chr22:46195948
|
G | A | 11 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0005g0009others(8): Show | 11 | HG00639.hp1 HG01167.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.-42-2394G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46195948 | ||||||
| chr22:46196046
|
G | A | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-2296G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196046 | ||||||
| chr22:46196078
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-42-2264C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196078 | ||||||
| chr22:46196084
|
C | T | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-42-2258C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196084 | ||||||
| chr22:46196106
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-42-2236G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196106 | ||||||
| chr22:46196195
|
C | T | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-2147C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196195 | ||||||
| chr22:46196202
|
A | G | 1 | a0001c0001t0025g0056 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-42-2140A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196202 | ||||||
| chr22:46196249
|
C | T | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-42-2093C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196249 | ||||||
| chr22:46196271
|
T | C | 40 | a0001c0001t0001g0125a0001c0001t0001g0193a0001c0001t0002g0185others(37): Show | 40 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.-42-2071T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196271 | ||||||
| chr22:46196425
|
C | T | 10 | a0001c0001t0001g0125a0001c0001t0001g0193a0001c0001t0004g0169others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42-1917C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196425 | ||||||
| chr22:46196487
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-42-1855C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196487 | ||||||
| chr22:46196522
|
C | T | 1 | a0001c0004t0001g0055 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-42-1820C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196522 | ||||||
| chr22:46196527
|
C | T | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-42-1815C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196527 | ||||||
| chr22:46196630
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0015g0019a0001c0001t0069g0161 | 3 | HG01243.hp2 HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-42-1712G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196630 | ||||||
| chr22:46196655
|
G | A | 1 | a0001c0001t0015g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-42-1687G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196655 | ||||||
| chr22:46196661
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-42-1681C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196661 | ||||||
| chr22:46196869
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-42-1473C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196869 | ||||||
| chr22:46196925
|
G | C | 10 | a0001c0001t0002g0195a0001c0001t0005g0011a0001c0001t0005g0028others(7): Show | 10 | HG00738.hp2 HG01069.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42-1417G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46196925 | ||||||
| chr22:46197029
|
TGTTTGGT others(10): Show |
T | 8 | a0001c0001t0002g0098a0001c0001t0004g0051a0001c0001t0004g0151others(5): Show | 8 | HG01943.hp2 HG02145.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-1296_-42-1280d others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46197029 | |||||
| chr22:46197065
|
T | G | 1 | a0001c0001t0016g0027 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-42-1277T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197065 | ||||||
| chr22:46197074
|
C | T | 4 | a0001c0001t0004g0051a0001c0001t0004g0151a0001c0001t0004g0172others(1): Show | 4 | HG01943.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-1268C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197074 | ||||||
| chr22:46197094
|
G | A | 2 | a0001c0001t0051g0024a0003c0003t0059g0045 | 2 | HG00639.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-42-1248G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197094 | ||||||
| chr22:46197206
|
C | T | 10 | a0001c0001t0002g0098a0001c0001t0004g0051a0001c0001t0004g0151others(7): Show | 10 | HG01433.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42-1136C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197206 | ||||||
| chr22:46197207
|
A | G | 73 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(70): Show | 73 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.-42-1135A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197207 | ||||||
| chr22:46197209
|
C | G | 8 | a0001c0001t0002g0098a0001c0001t0004g0051a0001c0001t0004g0151others(5): Show | 8 | HG01943.hp2 HG02145.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-1133C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197209 | ||||||
| chr22:46197268
|
T | C | 1 | a0001c0001t0037g0064 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-42-1074T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197268 | ||||||
| chr22:46197281
|
C | G | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-42-1061C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197281 | ||||||
| chr22:46197339
|
T | C | 81 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0090others(78): Show | 81 | HG00597.hp1 HG00639.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.-42-1003T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197339 | ||||||
| chr22:46197340
|
G | A | 1 | a0001c0001t0020g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-42-1002G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197340 | ||||||
| chr22:46197386
|
C | T | 10 | a0001c0001t0002g0098a0001c0001t0004g0051a0001c0001t0004g0151others(7): Show | 10 | HG01433.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42-956C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197386 | ||||||
| chr22:46197402
|
C | T | 8 | a0001c0001t0002g0098a0001c0001t0004g0051a0001c0001t0004g0151others(5): Show | 8 | HG01943.hp2 HG02145.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-940C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197402 | ||||||
| chr22:46197439
|
A | T | 38 | a0001c0001t0001g0125a0001c0001t0001g0193a0001c0001t0002g0185others(35): Show | 38 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-42-903A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197439 | ||||||
| chr22:46197828
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0007g0036 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-42-514C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197828 | ||||||
| chr22:46197879
|
G | A | 2 | a0001c0001t0017g0100a0001c0001t0068g0119 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42-463G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197879 | ||||||
| chr22:46197921
|
A | T | 19 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-42-421A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46197921 | ||||||
| chr22:46198014
|
G | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.-42-328G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198014 | ||||||
| chr22:46198038
|
T | C | 69 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(66): Show | 69 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.-42-304T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198038 | ||||||
| chr22:46198039
|
G | A | 7 | a0001c0001t0005g0011a0001c0001t0005g0028a0001c0001t0005g0115others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42-303G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198039 | ||||||
| chr22:46198045
|
C | T | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-42-297C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198045 | ||||||
| chr22:46198048
|
A | G | 3 | a0001c0001t0051g0024a0003c0003t0010g0043a0003c0003t0059g0045 | 3 | HG00639.hp1 HG01167.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-42-294A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198048 | ||||||
| chr22:46198058
|
G | A | 2 | a0001c0001t0004g0169a0001c0001t0007g0036 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-42-284G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198058 | ||||||
| chr22:46198066
|
T | TA | 27 | a0001c0001t0001g0193a0001c0001t0002g0185a0001c0001t0002g0195others(24): Show | 27 | HG00438.hp1 HG01109.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.-42-263dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46198066 | |||||
| chr22:46198106
|
C | T | 7 | a0001c0001t0005g0011a0001c0001t0005g0028a0001c0001t0005g0115others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42-236C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198106 | ||||||
| chr22:46198115
|
G | A | 8 | a0001c0001t0002g0098a0001c0001t0004g0051a0001c0001t0004g0151others(5): Show | 8 | HG01943.hp2 HG02145.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-227G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198115 | ||||||
| chr22:46198138
|
T | C | 25 | a0001c0001t0001g0125a0001c0001t0002g0185a0001c0001t0002g0195others(22): Show | 25 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-42-204T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198138 | ||||||
| chr22:46198192
|
T | C | 77 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(74): Show | 77 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.-42-150T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198192 | ||||||
| chr22:46198211
|
C | A | 1 | a0001c0001t0002g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-42-131C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198211 | ||||||
| chr22:46198237
|
C | CAAAA | 6 | a0001c0001t0005g0011a0001c0001t0005g0115a0001c0001t0005g0130others(3): Show | 6 | HG00738.hp2 HG01516.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42-92_-42-89dupAA others(2): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46198237 | |||||
| chr22:46198237
|
C | CAAAAAA | 13 | a0001c0001t0001g0122a0001c0001t0007g0020a0001c0001t0011g0034others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-42-94_-42-89dupAA others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46198237 | |||||
| chr22:46198237
|
C | CAAAAAAA | 29 | a0001c0001t0001g0125a0001c0001t0001g0193a0001c0001t0002g0098others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.-42-95_-42-89dupAA others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46198237 | |||||
| chr22:46198237
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0002g0195a0001c0001t0006g0153a0001c0001t0016g0027others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42-96_-42-89dupAA others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46198237 | |||||
| chr22:46198237
|
C | CAAAAAAA others(2): Show |
15 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0171others(12): Show | 15 | HG00639.hp1 HG01167.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-42-97_-42-89dupAA others(7): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46198237 | |||||
| chr22:46198237
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0148 | 2 | HG01978.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-42-98_-42-89dupAA others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 46198237 | |||||
| chr22:46198266
|
A | G | 6 | a0001c0001t0001g0193a0001c0001t0018g0186a0001c0001t0018g0187others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42-76A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 3/8 | chr22 | 46198266 | ||||||
| chr22:46198658
|
C | CT | 6 | a0001c0001t0001g0090a0001c0001t0004g0169a0001c0001t0014g0048others(3): Show | 6 | HG00438.hp1 HG01167.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+87dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46198658 | |||||
| chr22:46198658
|
C | CTT | 45 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0122others(42): Show | 45 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.208+86_208+87dupTT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46198658 | |||||
| chr22:46198658
|
C | CTTT | 10 | a0001c0001t0001g0125a0001c0001t0006g0153a0001c0001t0007g0020others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+85_208+87dupTT others(1): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46198658 | |||||
| chr22:46198698
|
T | C | 1 | a0002c0002t0002g0164 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.208+107T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46198698 | ||||||
| chr22:46198700
|
G | A | 1 | a0002c0002t0002g0164 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.208+109G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46198700 | ||||||
| chr22:46198715
|
C | CAATA | 2 | a0001c0001t0001g0053a0001c0001t0019g0088 | 2 | HG01358.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.208+127_208+128ins others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46198715 | |||||
| chr22:46198741
|
G | A | 74 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(71): Show | 74 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.208+150G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46198741 | ||||||
| chr22:46198835
|
A | G | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.208+244A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46198835 | ||||||
| chr22:46198853
|
G | T | 108 | a0001c0001t0001g0073a0001c0001t0001g0080a0001c0001t0001g0090others(105): Show | 108 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(105): Show |
intron_variant | MODIFIER | c.208+262G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46198853 | ||||||
| chr22:46199061
|
G | A | 8 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+470G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199061 | ||||||
| chr22:46199136
|
G | A | 33 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(30): Show | 33 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.208+545G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199136 | ||||||
| chr22:46199138
|
A | G | 65 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(62): Show | 65 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.208+547A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199138 | ||||||
| chr22:46199219
|
G | GTTGCAGA others(4): Show |
1 | a0001c0001t0025g0056 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.208+629_208+630ins others(11): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46199219 | |||||
| chr22:46199221
|
C | A | 1 | a0001c0001t0025g0056 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.208+630C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199221 | ||||||
| chr22:46199372
|
C | G | 1 | a0001c0001t0070g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.208+781C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199372 | ||||||
| chr22:46199481
|
A | T | 3 | a0001c0001t0003g0025a0001c0001t0003g0103a0001c0001t0062g0026 | 3 | HG02559.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.208+890A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199481 | ||||||
| chr22:46199487
|
A | T | 4 | a0001c0001t0003g0147a0001c0001t0018g0097a0001c0001t0018g0186others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+896A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199487 | ||||||
| chr22:46199649
|
A | T | 25 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0090others(22): Show | 25 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.208+1058A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199649 | ||||||
| chr22:46199684
|
C | G | 1 | a0001c0001t0062g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.208+1093C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199684 | ||||||
| chr22:46199795
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.208+1204C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46199795 | ||||||
| chr22:46200205
|
C | T | 1 | a0001c0001t0007g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.208+1614C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200205 | ||||||
| chr22:46200239
|
G | T | 6 | a0001c0001t0004g0051a0001c0001t0004g0151a0001c0001t0004g0172others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+1648G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200239 | ||||||
| chr22:46200348
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.208+1757G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200348 | ||||||
| chr22:46200349
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.208+1758A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200349 | ||||||
| chr22:46200376
|
T | C | 12 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1785T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200376 | ||||||
| chr22:46200399
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.208+1808G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200399 | ||||||
| chr22:46200466
|
C | T | 3 | a0001c0001t0020g0128a0001c0001t0073g0042a0001c0001t0074g0112 | 3 | HG02895.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+1875C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200466 | ||||||
| chr22:46200484
|
C | G | 1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+1893C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200484 | ||||||
| chr22:46200702
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.208+2111G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200702 | ||||||
| chr22:46200713
|
C | G | 1 | a0001c0001t0016g0027 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208+2122C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200713 | ||||||
| chr22:46200737
|
A | G | 16 | a0001c0001t0004g0051a0001c0001t0004g0151a0001c0001t0004g0172others(13): Show | 16 | HG01109.hp1 HG01943.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.208+2146A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200737 | ||||||
| chr22:46200789
|
G | A | 1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+2198G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200789 | ||||||
| chr22:46200836
|
A | T | 1 | a0001c0001t0034g0158 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.208+2245A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200836 | ||||||
| chr22:46200891
|
T | A | 6 | a0001c0001t0004g0051a0001c0001t0004g0151a0001c0001t0004g0172others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+2300T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46200891 | ||||||
| chr22:46201094
|
A | G | 1 | a0001c0001t0016g0027 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208+2503A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201094 | ||||||
| chr22:46201124
|
C | CA | 28 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(25): Show | 28 | HG01109.hp1 HG01891.hp2 HG01943.hp2 others(25): Show |
intron_variant | MODIFIER | c.208+2552dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46201124 | |||||
| chr22:46201124
|
CA | C | 5 | a0001c0001t0001g0071a0001c0001t0014g0048a0001c0001t0017g0100others(2): Show | 5 | HG02165.hp1 HG02165.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+2552delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46201124 | |||||
| chr22:46201249
|
C | T | 1 | a0001c0001t0025g0056 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.208+2658C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201249 | ||||||
| chr22:46201390
|
A | C | 6 | a0001c0001t0002g0098a0001c0001t0006g0143a0001c0001t0012g0083others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+2799A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201390 | ||||||
| chr22:46201414
|
G | C | 1 | a0001c0001t0002g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.208+2823G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201414 | ||||||
| chr22:46201415
|
C | T | 2 | a0001c0001t0020g0178a0001c0001t0057g0157 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.208+2824C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201415 | ||||||
| chr22:46201627
|
T | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.208+3036T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201627 | ||||||
| chr22:46201776
|
C | G | 8 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0015g0136others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+3185C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201776 | ||||||
| chr22:46201831
|
G | A | 1 | a0001c0001t0020g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.208+3240G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201831 | ||||||
| chr22:46201880
|
T | C | 4 | a0001c0001t0029g0003a0001c0001t0029g0162a0001c0001t0077g0004others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+3289T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201880 | ||||||
| chr22:46201962
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.208+3371C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46201962 | ||||||
| chr22:46202045
|
G | C | 2 | a0001c0001t0029g0003a0001c0001t0029g0162 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.208+3454G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202045 | ||||||
| chr22:46202195
|
T | C | 1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+3604T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202195 | ||||||
| chr22:46202235
|
C | A | 4 | a0001c0001t0028g0118a0001c0001t0067g0022a0001c0001t0070g0168others(1): Show | 4 | HG02451.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+3644C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202235 | ||||||
| chr22:46202355
|
T | C | 1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+3764T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202355 | ||||||
| chr22:46202410
|
A | G | 74 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(71): Show | 74 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.208+3819A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202410 | ||||||
| chr22:46202606
|
CGTG | C | 3 | a0001c0001t0018g0097a0001c0001t0018g0186a0001c0001t0018g0187 | 3 | HG01167.hp1 HG01169.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.208+4016_208+4018d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202606 | ||||||
| chr22:46202612
|
C | G | 3 | a0001c0001t0018g0097a0001c0001t0018g0186a0001c0001t0018g0187 | 3 | HG01167.hp1 HG01169.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.208+4021C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202612 | ||||||
| chr22:46202728
|
C | T | 8 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+4137C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202728 | ||||||
| chr22:46202734
|
T | C | 90 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(87): Show | 90 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.208+4143T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202734 | ||||||
| chr22:46202794
|
C | T | 1 | a0001c0001t0018g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208+4203C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202794 | ||||||
| chr22:46202862
|
T | TTAAA | 13 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.208+4290_208+4293d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46202862 | |||||
| chr22:46202972
|
A | G | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208+4381A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46202972 | ||||||
| chr22:46203050
|
C | T | 56 | a0001c0001t0001g0125a0001c0001t0002g0098a0001c0001t0003g0101others(53): Show | 56 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(53): Show |
intron_variant | MODIFIER | c.208+4459C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46203050 | ||||||
| chr22:46203070
|
A | G | 2 | a0001c0001t0006g0143a0001c0001t0012g0083 | 2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.208+4479A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46203070 | ||||||
| chr22:46203253
|
T | A | 1 | a0001c0001t0077g0004 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+4662T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46203253 | ||||||
| chr22:46203802
|
C | A | 1 | a0002c0002t0044g0023 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.208+5211C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46203802 | ||||||
| chr22:46203951
|
CTCTG | C | 4 | a0001c0001t0028g0118a0001c0001t0067g0022a0001c0001t0070g0168others(1): Show | 4 | HG02451.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+5367_208+5370d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46203951 | |||||
| chr22:46203959
|
G | A | 8 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0169others(5): Show | 8 | HG01433.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+5368G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46203959 | ||||||
| chr22:46204011
|
G | A | 20 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(17): Show | 20 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.208+5420G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46204011 | ||||||
| chr22:46204210
|
T | C | 21 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(18): Show | 21 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.208+5619T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46204210 | ||||||
| chr22:46204281
|
A | G | 7 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0015g0136others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+5690A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46204281 | ||||||
| chr22:46204315
|
A | G | 2 | a0001c0001t0020g0178a0001c0001t0057g0157 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.208+5724A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46204315 | ||||||
| chr22:46204837
|
T | TA | 23 | a0001c0001t0002g0145a0001c0001t0006g0106a0001c0001t0006g0134others(20): Show | 23 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.208+6258dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46204837 | |||||
| chr22:46204850
|
GA | G | 3 | a0001c0001t0004g0038a0001c0001t0017g0100a0001c0001t0068g0119 | 3 | HG02723.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.208+6265delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46204850 | |||||
| chr22:46204961
|
G | A | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+6370G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46204961 | ||||||
| chr22:46204978
|
C | T | 1 | a0001c0001t0020g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.208+6387C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46204978 | ||||||
| chr22:46204991
|
C | T | 20 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(17): Show | 20 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.208+6400C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46204991 | ||||||
| chr22:46205160
|
G | A | 20 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(17): Show | 20 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.208+6569G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205160 | ||||||
| chr22:46205167
|
TC | T | 8 | a0001c0001t0002g0191a0001c0001t0003g0021a0001c0001t0003g0025others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+6577delC | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205167 | ||||||
| chr22:46205248
|
C | T | 7 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+6657C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205248 | ||||||
| chr22:46205360
|
G | T | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+6769G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205360 | ||||||
| chr22:46205508
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0015g0136 | 2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.208+6917C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205508 | ||||||
| chr22:46205519
|
C | CAT | 6 | a0001c0001t0001g0096a0001c0001t0002g0063a0001c0001t0009g0175others(3): Show | 6 | HG00438.hp2 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+6963_208+6964d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205519 | |||||
| chr22:46205519
|
C | CATATAT | 2 | a0001c0001t0004g0049a0001c0001t0004g0060 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.208+6959_208+6964d others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205519 | |||||
| chr22:46205519
|
CAT | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0084a0001c0001t0012g0083others(2): Show | 5 | HG01516.hp1 HG02698.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+6963_208+6964d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205519 | |||||
| chr22:46205519
|
CATAT | C | 4 | a0001c0001t0014g0046a0001c0001t0018g0097a0001c0001t0079g0107others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+6961_208+6964d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205519 | |||||
| chr22:46205519
|
CATATATA others(1): Show |
C | 2 | a0001c0001t0020g0178a0001c0001t0058g0079 | 2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.208+6957_208+6964d others(10): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205519 | |||||
| chr22:46205519
|
CATATATA others(7): Show |
C | 4 | a0001c0001t0003g0101a0001c0001t0028g0118a0001c0001t0067g0022others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+6951_208+6964d others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205519 | |||||
| chr22:46205519
|
CATATATA others(9): Show |
C | 1 | a0003c0003t0059g0045 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.208+6949_208+6964d others(18): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205519 | |||||
| chr22:46205519
|
CATATATA others(11): Show |
C | 11 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(8): Show | 11 | HG01433.hp2 HG01496.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.208+6947_208+6964d others(20): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205519 | |||||
| chr22:46205530
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0017g0062 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.208+6941_208+6969d others(31): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205530 | |||||
| chr22:46205532
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0068g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.208+6943_208+6965d others(25): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205532 | |||||
| chr22:46205532
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0017g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208+6943_208+6966d others(26): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205532 | |||||
| chr22:46205534
|
ATATATAT others(23): Show |
A | 1 | a0003c0003t0010g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.208+6945_208+6974d others(32): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205534 | |||||
| chr22:46205535
|
TATATATA others(8): Show |
T | 2 | a0003c0003t0010g0043a0003c0003t0036g0013 | 2 | HG01433.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.208+6945_208+6959d others(17): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205535 | ||||||
| chr22:46205536
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0014g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208+6947_208+6965d others(21): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205536 | |||||
| chr22:46205537
|
TATATATA others(6): Show |
T | 2 | a0001c0001t0001g0090a0001c0001t0003g0102 | 2 | HG01978.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.208+6947_208+6959d others(15): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205537 | ||||||
| chr22:46205539
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0003g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.208+6949_208+6961d others(15): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205539 | ||||||
| chr22:46205540
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0023g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.208+6951_208+6967d others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205540 | |||||
| chr22:46205542
|
ATATATAT others(7): Show |
A | 9 | a0001c0001t0006g0106a0001c0001t0006g0134a0001c0001t0006g0153others(6): Show | 9 | HG01109.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.208+6953_208+6966d others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205542 | |||||
| chr22:46205542
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0077g0004 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+6953_208+6967d others(17): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205542 | |||||
| chr22:46205544
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0063g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.208+6955_208+6965d others(13): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205544 | |||||
| chr22:46205544
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0006g0029a0001c0001t0035g0163 | 2 | HG02451.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.208+6955_208+6966d others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205544 | |||||
| chr22:46205546
|
A | G | 1 | a0001c0006t0026g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+6955A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205546 | ||||||
| chr22:46205548
|
A | G | 1 | a0001c0001t0009g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.208+6957A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205548 | ||||||
| chr22:46205548
|
A | T | 2 | a0001c0001t0018g0097a0001c0001t0020g0128 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.208+6957A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205548 | ||||||
| chr22:46205549
|
TA | T | 2 | a0001c0001t0002g0117a0001c0001t0054g0089 | 2 | HG02145.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.208+6959delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205549 | ||||||
| chr22:46205550
|
A | AT | 3 | a0001c0001t0001g0086a0001c0001t0061g0188a0001c0001t0071g0010 | 3 | HG01934.hp1 HG02273.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.208+6960dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205550 | |||||
| chr22:46205550
|
A | G | 1 | a0001c0006t0032g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.208+6959A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205550 | ||||||
| chr22:46205550
|
A | T | 5 | a0001c0001t0001g0052a0001c0001t0002g0166a0001c0001t0018g0097others(2): Show | 5 | HG01943.hp1 HG03130.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+6959A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205550 | ||||||
| chr22:46205550
|
ATATATTT others(5): Show |
A | 1 | a0001c0001t0029g0162 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208+6961_208+6972d others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205550 | |||||
| chr22:46205551
|
TA | T | 6 | a0001c0001t0001g0193a0001c0001t0002g0108a0001c0001t0024g0181others(3): Show | 6 | HG02155.hp2 HG02523.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+6961delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205551 | ||||||
| chr22:46205552
|
A | AT | 3 | a0001c0001t0001g0057a0001c0001t0049g0092a0002c0002t0056g0179 | 3 | HG02071.hp2 NA18948.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.208+6962dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205552 | |||||
| chr22:46205552
|
A | T | 25 | a0001c0001t0001g0052a0001c0001t0001g0072a0001c0001t0001g0086others(22): Show | 25 | HG00597.hp1 HG00639.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.208+6961A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205552 | ||||||
| chr22:46205552
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0029g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.208+6963_208+6974d others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205552 | |||||
| chr22:46205553
|
TA | T | 17 | a0001c0001t0001g0015a0001c0001t0001g0071a0001c0001t0001g0087others(14): Show | 17 | HG00438.hp1 HG01106.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+6963delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205553 | ||||||
| chr22:46205554
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0002g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.208+6964_208+6965i others(23): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+6964_208+6965i others(41): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(40): Show |
2 | a0001c0001t0018g0186a0001c0001t0018g0187 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.208+6964_208+6965i others(49): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0015g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208+6964_208+6965i others(31): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0038g0126 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.208+6964_208+6965i others(27): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0005g0011 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.208+6964_208+6965i others(28): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0005g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.208+6964_208+6965i others(26): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208+6964_208+6965i others(24): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0005g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.208+6964_208+6965i others(26): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.208+6964_208+6965i others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0005g0028 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.208+6964_208+6965i others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0008g0199a0001c0001t0031g0198 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.208+6964_208+6965i others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0005g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.208+6964_208+6965i others(21): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0039 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208+6964_208+6965i others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0073g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.208+6964_208+6965i others(14): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | ATT | 7 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0070others(4): Show | 7 | HG00099.hp1 HG00597.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+6992_208+6993d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
A | T | 53 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0072others(50): Show | 53 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.208+6963A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205554 | ||||||
| chr22:46205554
|
AT | A | 13 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0139others(10): Show | 13 | HG00738.hp1 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.208+6993delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205554
|
ATT | A | 12 | a0001c0001t0001g0110a0001c0001t0001g0122a0001c0001t0003g0103others(9): Show | 12 | HG01358.hp1 HG01934.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+6992_208+6993d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46205554 | |||||
| chr22:46205555
|
T | TA | 7 | a0001c0001t0001g0184a0001c0001t0002g0189a0001c0001t0007g0020others(4): Show | 7 | HG02071.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+6964_208+6965i others(3): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205555 | ||||||
| chr22:46205555
|
T | TATA | 5 | a0001c0001t0001g0138a0001c0001t0001g0171a0001c0001t0004g0038others(2): Show | 6 | HG01071.hp1 HG01169.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+6964_208+6965i others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205555 | ||||||
| chr22:46205555
|
T | TATATATA others(10): Show |
2 | a0001c0001t0007g0135a0001c0001t0040g0074 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.208+6964_208+6965i others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205555 | ||||||
| chr22:46205556
|
T | A | 3 | a0001c0001t0004g0049a0001c0001t0004g0060a0001c0001t0064g0159 | 3 | HG01884.hp1 HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.208+6965T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205556 | ||||||
| chr22:46205557
|
T | A | 7 | a0001c0001t0001g0073a0001c0001t0007g0020a0001c0001t0007g0036others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+6966T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205557 | ||||||
| chr22:46205558
|
T | A | 6 | a0001c0001t0011g0094a0001c0001t0016g0160a0001c0001t0016g0194others(3): Show | 6 | HG01884.hp1 HG01934.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+6967T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205558 | ||||||
| chr22:46205559
|
T | A | 3 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0017g0061 | 3 | HG02280.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.208+6968T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205559 | ||||||
| chr22:46205560
|
T | A | 2 | a0001c0001t0064g0159a0001c0001t0065g0047 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.208+6969T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205560 | ||||||
| chr22:46205728
|
G | A | 18 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(15): Show | 18 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+7137G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205728 | ||||||
| chr22:46205791
|
G | C | 1 | a0001c0001t0020g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.208+7200G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205791 | ||||||
| chr22:46205872
|
G | C | 19 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(16): Show | 19 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.208+7281G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205872 | ||||||
| chr22:46205985
|
A | G | 1 | a0001c0001t0020g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.208+7394A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46205985 | ||||||
| chr22:46206014
|
A | G | 22 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(19): Show | 22 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.208+7423A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206014 | ||||||
| chr22:46206031
|
C | T | 1 | a0001c0001t0020g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.208+7440C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206031 | ||||||
| chr22:46206125
|
C | T | 7 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0015g0136others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+7534C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206125 | ||||||
| chr22:46206270
|
TTG | T | 22 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0145others(19): Show | 22 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.208+7699_208+7700d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46206270 | |||||
| chr22:46206270
|
TTGTG | T | 53 | a0001c0001t0001g0125a0001c0001t0002g0098a0001c0001t0003g0101others(50): Show | 53 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.208+7697_208+7700d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46206270 | |||||
| chr22:46206389
|
A | G | 7 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0015g0136others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+7798A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206389 | ||||||
| chr22:46206506
|
G | A | 9 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(6): Show | 9 | HG01109.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+7915G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206506 | ||||||
| chr22:46206750
|
A | G | 12 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(9): Show | 12 | HG01433.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+8159A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206750 | ||||||
| chr22:46206960
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.209-8213C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206960 | ||||||
| chr22:46206988
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.209-8185C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206988 | ||||||
| chr22:46206993
|
C | T | 1 | a0001c0001t0014g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209-8180C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46206993 | ||||||
| chr22:46207155
|
A | G | 1 | a0001c0001t0050g0078 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.209-8018A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207155 | ||||||
| chr22:46207179
|
C | T | 2 | a0001c0001t0014g0046a0001c0001t0079g0107 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.209-7994C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207179 | ||||||
| chr22:46207277
|
A | AT | 9 | a0001c0001t0001g0057a0001c0001t0001g0086a0001c0001t0002g0075others(6): Show | 9 | HG00597.hp2 HG01934.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-7874dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207277 | |||||
| chr22:46207277
|
AT | A | 32 | a0001c0001t0001g0125a0001c0001t0001g0174a0001c0001t0002g0098others(29): Show | 32 | HG01069.hp1 HG01243.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.209-7874delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207277 | |||||
| chr22:46207277
|
ATT | A | 16 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0145others(13): Show | 16 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.209-7875_209-7874d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207277 | |||||
| chr22:46207277
|
ATTT | A | 9 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(6): Show | 9 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-7876_209-7874d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207277 | |||||
| chr22:46207277
|
ATTTT | A | 18 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(15): Show | 18 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.209-7877_209-7874d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207277 | |||||
| chr22:46207348
|
C | A | 8 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-7825C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207348 | ||||||
| chr22:46207419
|
T | C | 48 | a0001c0001t0002g0098a0001c0001t0003g0101a0001c0001t0003g0102others(45): Show | 48 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.209-7754T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207419 | ||||||
| chr22:46207427
|
A | G | 56 | a0001c0001t0001g0125a0001c0001t0002g0098a0001c0001t0003g0101others(53): Show | 56 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(53): Show |
intron_variant | MODIFIER | c.209-7746A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207427 | ||||||
| chr22:46207442
|
C | T | 6 | a0001c0001t0002g0098a0001c0001t0006g0143a0001c0001t0012g0083others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-7731C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207442 | ||||||
| chr22:46207531
|
C | T | 1 | a0001c0001t0010g0182 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.209-7642C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207531 | ||||||
| chr22:46207644
|
T | TTTA | 3 | a0001c0001t0029g0003a0001c0001t0029g0162a0001c0001t0048g0140 | 3 | HG00438.hp1 HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.209-7496_209-7494d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207644 | |||||
| chr22:46207644
|
TTTA | T | 10 | a0001c0001t0001g0125a0001c0001t0006g0029a0001c0001t0006g0134others(7): Show | 10 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-7496_209-7494d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207644 | |||||
| chr22:46207644
|
TTTATTA | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0015g0136others(1): Show | 4 | HG02257.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-7499_209-7494d others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207644 | |||||
| chr22:46207644
|
TTTATTAT others(8): Show |
T | 1 | a0001c0001t0041g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209-7508_209-7494d others(17): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207644 | |||||
| chr22:46207644
|
TTTATTAT others(11): Show |
T | 6 | a0001c0001t0002g0098a0001c0001t0006g0143a0001c0001t0012g0083others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-7511_209-7494d others(20): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207644 | |||||
| chr22:46207653
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.209-7520A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207653 | ||||||
| chr22:46207656
|
A | T | 1 | a0001c0001t0015g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209-7517A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207656 | ||||||
| chr22:46207665
|
ATTATTAT others(13): Show |
A | 3 | a0001c0001t0020g0178a0001c0001t0057g0157a0001c0001t0075g0006 | 3 | HG02572.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.209-7505_209-7486d others(22): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207665 | |||||
| chr22:46207668
|
ATTATTAT others(11): Show |
A | 3 | a0001c0001t0004g0169a0001c0001t0014g0048a0001c0001t0058g0079 | 3 | HG01433.hp2 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.209-7502_209-7485d others(20): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207668 | |||||
| chr22:46207670
|
TATTA | T | 2 | a0001c0001t0001g0073a0001c0001t0020g0128 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.209-7502_209-7499d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207670 | ||||||
| chr22:46207671
|
A | AT | 4 | a0001c0001t0001g0008a0001c0001t0012g0005a0001c0001t0022g0067others(1): Show | 4 | HG01167.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-7500dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207671 | |||||
| chr22:46207671
|
A | T | 8 | a0001c0001t0004g0038a0001c0001t0008g0167a0001c0001t0016g0160others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-7502A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207671 | ||||||
| chr22:46207671
|
ATTATTAT others(11): Show |
A | 11 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-7499_209-7482d others(20): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207671 | |||||
| chr22:46207674
|
A | ATTT | 8 | a0001c0001t0001g0095a0001c0001t0002g0082a0001c0001t0002g0170others(5): Show | 8 | HG00597.hp1 HG00738.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-7497_209-7496i others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207674 | |||||
| chr22:46207674
|
A | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0053others(31): Show | 34 | HG00738.hp1 HG01167.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.209-7499A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207674 | ||||||
| chr22:46207674
|
ATTATTTT others(11): Show |
A | 7 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-7496_209-7479d others(20): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207674 | |||||
| chr22:46207677
|
A | ATT | 6 | a0001c0001t0002g0185a0001c0001t0005g0028a0001c0001t0007g0120others(3): Show | 6 | HG01069.hp1 HG01943.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-7474_209-7473d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207677 | |||||
| chr22:46207677
|
A | ATTATTAT others(3): Show |
1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.209-7494_209-7493i others(12): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207677 | |||||
| chr22:46207677
|
A | ATTT | 16 | a0001c0001t0001g0068a0001c0001t0001g0096a0001c0001t0001g0148others(13): Show | 16 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-7475_209-7473d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46207677 | |||||
| chr22:46207677
|
A | T | 89 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(86): Show | 89 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.209-7496A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207677 | ||||||
| chr22:46207680
|
T | A | 7 | a0001c0001t0001g0072a0001c0001t0029g0003a0001c0001t0029g0162others(4): Show | 8 | HG00438.hp1 HG01071.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-7493T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207680 | ||||||
| chr22:46207681
|
T | A | 2 | a0001c0006t0026g0142a0001c0006t0032g0132 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.209-7492T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207681 | ||||||
| chr22:46207683
|
T | A | 6 | a0001c0001t0020g0128a0001c0001t0030g0001a0001c0001t0048g0140others(3): Show | 7 | HG00438.hp1 HG01071.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-7490T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207683 | ||||||
| chr22:46207684
|
T | A | 1 | a0001c0001t0001g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.209-7489T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207684 | ||||||
| chr22:46207685
|
T | A | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.209-7488T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207685 | ||||||
| chr22:46207686
|
T | A | 1 | a0001c0001t0052g0066 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.209-7487T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207686 | ||||||
| chr22:46207688
|
T | A | 1 | a0001c0001t0020g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.209-7485T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207688 | ||||||
| chr22:46207717
|
G | A | 1 | a0001c0001t0055g0155 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.209-7456G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207717 | ||||||
| chr22:46207750
|
C | T | 1 | a0001c0001t0010g0182 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.209-7423C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207750 | ||||||
| chr22:46207954
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.209-7219G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207954 | ||||||
| chr22:46207996
|
A | C | 1 | a0001c0001t0013g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.209-7177A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46207996 | ||||||
| chr22:46208335
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.209-6838G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208335 | ||||||
| chr22:46208429
|
T | G | 9 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(6): Show | 9 | HG01109.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-6744T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208429 | ||||||
| chr22:46208500
|
A | G | 30 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(27): Show | 30 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-6673A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208500 | ||||||
| chr22:46208547
|
CA | C | 37 | a0001c0001t0001g0018a0001c0001t0001g0068a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.209-6609delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46208547 | |||||
| chr22:46208644
|
A | T | 3 | a0001c0001t0020g0178a0001c0001t0057g0157a0001c0001t0075g0006 | 3 | HG02572.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.209-6529A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208644 | ||||||
| chr22:46208899
|
CGT | C | 30 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(27): Show | 30 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-6258_209-6257d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46208899 | |||||
| chr22:46208915
|
T | C | 19 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(16): Show | 19 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-6258T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208915 | ||||||
| chr22:46208915
|
T | TGTGC | 2 | a0001c0001t0007g0135a0001c0001t0040g0074 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.209-6257_209-6256i others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46208915 | |||||
| chr22:46208917
|
C | T | 15 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.209-6256C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208917 | ||||||
| chr22:46208917
|
CGT | C | 18 | a0001c0001t0002g0098a0001c0001t0003g0124a0001c0001t0004g0037others(15): Show | 18 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-6239_209-6238d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46208917 | |||||
| chr22:46208917
|
CGTGTGT | C | 19 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(16): Show | 19 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-6243_209-6238d others(8): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46208917 | |||||
| chr22:46208919
|
T | C | 42 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(39): Show | 42 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.209-6254T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208919 | ||||||
| chr22:46208946
|
CT | C | 2 | a0001c0006t0026g0142a0001c0006t0032g0132 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.209-6224delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46208946 | |||||
| chr22:46208958
|
G | A | 52 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(49): Show | 52 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.209-6215G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208958 | ||||||
| chr22:46208980
|
T | A | 1 | a0004c0008t0009g0146 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.209-6193T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46208980 | ||||||
| chr22:46209045
|
C | G | 5 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0015g0136others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-6128C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209045 | ||||||
| chr22:46209207
|
A | G | 82 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(79): Show | 82 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.209-5966A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209207 | ||||||
| chr22:46209222
|
T | A | 1 | a0001c0001t0013g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.209-5951T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209222 | ||||||
| chr22:46209293
|
T | C | 57 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(54): Show | 57 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.209-5880T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209293 | ||||||
| chr22:46209329
|
G | T | 1 | a0001c0001t0013g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.209-5844G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209329 | ||||||
| chr22:46209455
|
A | T | 1 | a0001c0001t0013g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.209-5718A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209455 | ||||||
| chr22:46209473
|
AT | A | 79 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(76): Show | 79 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.209-5698delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46209473 | |||||
| chr22:46209491
|
T | C | 12 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-5682T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209491 | ||||||
| chr22:46209645
|
T | A | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.209-5528T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209645 | ||||||
| chr22:46209677
|
G | C | 1 | a0001c0001t0027g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.209-5496G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209677 | ||||||
| chr22:46209690
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0050g0078a0001c0004t0001g0055others(1): Show | 4 | NA18999.hp1 NA19004.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-5483A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209690 | ||||||
| chr22:46209732
|
G | T | 13 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(10): Show | 13 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-5441G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209732 | ||||||
| chr22:46209750
|
G | A | 3 | a0001c0001t0020g0178a0001c0001t0057g0157a0001c0001t0075g0006 | 3 | HG02572.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.209-5423G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46209750 | ||||||
| chr22:46210008
|
G | A | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.209-5165G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210008 | ||||||
| chr22:46210099
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.209-5074C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210099 | ||||||
| chr22:46210100
|
G | A | 9 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-5073G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210100 | ||||||
| chr22:46210146
|
C | T | 68 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0098others(65): Show | 68 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-5027C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210146 | ||||||
| chr22:46210147
|
A | C | 5 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0015g0136others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-5026A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210147 | ||||||
| chr22:46210198
|
A | C | 13 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-4975A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210198 | ||||||
| chr22:46210234
|
G | T | 2 | a0001c0006t0026g0142a0001c0006t0032g0132 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.209-4939G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210234 | ||||||
| chr22:46210242
|
G | A | 49 | a0001c0001t0002g0098a0001c0001t0003g0101a0001c0001t0003g0102others(46): Show | 49 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.209-4931G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210242 | ||||||
| chr22:46210309
|
C | CA | 18 | a0001c0001t0001g0087a0001c0001t0001g0148a0001c0001t0001g0171others(15): Show | 18 | HG01496.hp1 HG01928.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-4844dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46210309 | |||||
| chr22:46210309
|
CA | C | 26 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0090others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.209-4844delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46210309 | |||||
| chr22:46210309
|
CAA | C | 29 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0124others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.209-4845_209-4844d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46210309 | |||||
| chr22:46210309
|
CAAA | C | 20 | a0001c0001t0002g0098a0001c0001t0006g0029a0001c0001t0006g0106others(17): Show | 20 | HG01496.hp2 HG02145.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.209-4846_209-4844d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46210309 | |||||
| chr22:46210442
|
T | G | 1 | a0001c0001t0001g0018 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.209-4731T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210442 | ||||||
| chr22:46210448
|
CT | C | 21 | a0001c0001t0001g0072a0001c0001t0006g0029a0001c0001t0006g0106others(18): Show | 21 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.209-4714delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46210448 | |||||
| chr22:46210497
|
C | T | 16 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0145others(13): Show | 16 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.209-4676C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210497 | ||||||
| chr22:46210498
|
G | A | 1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.209-4675G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210498 | ||||||
| chr22:46210724
|
A | G | 49 | a0001c0001t0002g0098a0001c0001t0003g0101a0001c0001t0003g0102others(46): Show | 49 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.209-4449A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210724 | ||||||
| chr22:46210733
|
C | T | 1 | a0001c0001t0053g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.209-4440C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210733 | ||||||
| chr22:46210948
|
G | A | 13 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-4225G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46210948 | ||||||
| chr22:46211144
|
C | T | 2 | a0001c0001t0035g0163a0001c0001t0063g0099 | 2 | HG03579.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.209-4029C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211144 | ||||||
| chr22:46211158
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.209-4015G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211158 | ||||||
| chr22:46211257
|
C | T | 13 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(10): Show | 13 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-3916C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211257 | ||||||
| chr22:46211258
|
G | A | 4 | a0001c0001t0028g0118a0001c0001t0067g0022a0001c0001t0070g0168others(1): Show | 4 | HG02451.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-3915G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211258 | ||||||
| chr22:46211322
|
A | G | 9 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-3851A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211322 | ||||||
| chr22:46211456
|
C | T | 14 | a0001c0001t0002g0098a0001c0001t0003g0101a0001c0001t0003g0102others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.209-3717C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211456 | ||||||
| chr22:46211481
|
A | G | 88 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(85): Show | 88 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.209-3692A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211481 | ||||||
| chr22:46211712
|
G | A | 19 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(16): Show | 19 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-3461G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211712 | ||||||
| chr22:46211716
|
T | C | 198 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.209-3457T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211716 | ||||||
| chr22:46211717
|
G | A | 2 | a0001c0001t0029g0003a0001c0001t0029g0162 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.209-3456G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211717 | ||||||
| chr22:46211755
|
G | A | 1 | a0001c0001t0009g0173 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.209-3418G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211755 | ||||||
| chr22:46211810
|
C | T | 66 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0098others(63): Show | 66 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-3363C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211810 | ||||||
| chr22:46211971
|
C | T | 1 | a0001c0001t0030g0001 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.209-3202C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46211971 | ||||||
| chr22:46212223
|
A | G | 12 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-2950A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46212223 | ||||||
| chr22:46212308
|
C | T | 3 | a0001c0001t0024g0180a0001c0001t0024g0181a0001c0001t0046g0154 | 3 | NA18948.hp2 NA19004.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.209-2865C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46212308 | ||||||
| chr22:46212338
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0086a0001c0001t0047g0012 | 3 | HG01109.hp2 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.209-2835T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46212338 | ||||||
| chr22:46212420
|
A | G | 1 | a0001c0001t0077g0004 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.209-2753A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46212420 | ||||||
| chr22:46212496
|
G | A | 1 | a0001c0001t0027g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.209-2677G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46212496 | ||||||
| chr22:46212821
|
C | T | 17 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(14): Show | 17 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-2352C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46212821 | ||||||
| chr22:46212853
|
G | A | 66 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0098others(63): Show | 66 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-2320G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46212853 | ||||||
| chr22:46212991
|
T | A | 19 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0145others(16): Show | 19 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-2182T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46212991 | ||||||
| chr22:46213021
|
T | A | 73 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0125others(70): Show | 73 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-2152T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46213021 | ||||||
| chr22:46213403
|
C | CT | 22 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0093others(19): Show | 22 | HG00099.hp2 HG01106.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.209-1753dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46213403 | |||||
| chr22:46213403
|
CT | C | 10 | a0001c0001t0001g0018a0001c0001t0003g0101a0001c0001t0003g0102others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-1753delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46213403 | |||||
| chr22:46213490
|
C | G | 13 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(10): Show | 13 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-1683C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46213490 | ||||||
| chr22:46213500
|
C | T | 1 | a0001c0001t0053g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.209-1673C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46213500 | ||||||
| chr22:46213597
|
CT | C | 23 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(20): Show | 23 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.209-1566delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46213597 | |||||
| chr22:46213675
|
C | T | 29 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0145others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.209-1498C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46213675 | ||||||
| chr22:46213882
|
C | T | 1 | a0001c0001t0049g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.209-1291C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46213882 | ||||||
| chr22:46213912
|
G | C | 1 | a0001c0001t0002g0082 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.209-1261G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46213912 | ||||||
| chr22:46214065
|
T | C | 3 | a0001c0001t0026g0152a0001c0006t0026g0142a0001c0006t0032g0132 | 3 | HG01891.hp1 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.209-1108T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214065 | ||||||
| chr22:46214170
|
G | A | 16 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0002g0145others(13): Show | 16 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.209-1003G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214170 | ||||||
| chr22:46214336
|
C | G | 23 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(20): Show | 23 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.209-837C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214336 | ||||||
| chr22:46214512
|
A | G | 90 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(87): Show | 90 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.209-661A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214512 | ||||||
| chr22:46214578
|
G | T | 2 | a0001c0001t0008g0199a0001c0001t0031g0198 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.209-595G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214578 | ||||||
| chr22:46214658
|
ACGGGTCC others(9): Show |
A | 3 | a0001c0001t0020g0178a0001c0001t0057g0157a0001c0001t0075g0006 | 3 | HG02572.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.209-502_209-487del others(16): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 46214658 | |||||
| chr22:46214746
|
G | A | 4 | a0001c0001t0006g0029a0001c0001t0006g0153a0001c0001t0006g0177others(1): Show | 4 | HG02451.hp2 HG02647.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-427G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214746 | ||||||
| chr22:46214832
|
G | A | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.209-341G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214832 | ||||||
| chr22:46214866
|
C | T | 8 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-307C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214866 | ||||||
| chr22:46214870
|
G | A | 17 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(14): Show | 17 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-303G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214870 | ||||||
| chr22:46214918
|
G | T | 4 | a0001c0001t0028g0118a0001c0001t0067g0022a0001c0001t0070g0168others(1): Show | 4 | HG02451.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-255G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214918 | ||||||
| chr22:46214928
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.209-245G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214928 | ||||||
| chr22:46214932
|
C | T | 13 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-241C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46214932 | ||||||
| chr22:46215090
|
C | T | 3 | a0001c0001t0020g0128a0001c0001t0029g0003a0001c0001t0029g0162 | 3 | HG02145.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.209-83C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46215090 | ||||||
| chr22:46215129
|
A | G | 2 | a0001c0001t0029g0003a0001c0001t0029g0162 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.209-44A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | chr22 | 46215129 | ||||||
| chr22:46215366
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0002g0075a0001c0001t0054g0089 | 3 | HG00597.hp2 HG02145.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.369+33G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46215366 | ||||||
| chr22:46215368
|
C | T | 2 | a0001c0006t0026g0142a0001c0006t0032g0132 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.369+35C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46215368 | ||||||
| chr22:46215536
|
G | C | 3 | a0001c0001t0020g0128a0001c0001t0073g0042a0001c0001t0074g0112 | 3 | HG02895.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.369+203G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46215536 | ||||||
| chr22:46215538
|
T | G | 65 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0090others(62): Show | 65 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.369+205T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46215538 | ||||||
| chr22:46215742
|
T | TA | 66 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(63): Show | 66 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.369+418dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46215742 | |||||
| chr22:46215831
|
C | T | 17 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(14): Show | 17 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.369+498C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46215831 | ||||||
| chr22:46215853
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.369+520G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46215853 | ||||||
| chr22:46215965
|
T | C | 1 | a0001c0001t0076g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.369+632T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46215965 | ||||||
| chr22:46215982
|
G | A | 1 | a0001c0001t0030g0001 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.369+649G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46215982 | ||||||
| chr22:46216053
|
G | A | 2 | a0001c0001t0029g0003a0001c0001t0029g0162 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.369+720G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216053 | ||||||
| chr22:46216104
|
C | T | 4 | a0001c0001t0004g0049a0001c0001t0004g0060a0001c0001t0007g0120others(1): Show | 4 | HG02559.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+771C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216104 | ||||||
| chr22:46216139
|
T | C | 23 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(20): Show | 23 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.369+806T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216139 | ||||||
| chr22:46216383
|
C | CAAAA | 12 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(9): Show | 12 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.369+1061_369+1064d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46216383 | |||||
| chr22:46216383
|
CA | C | 52 | a0001c0001t0001g0090a0001c0001t0002g0098a0001c0001t0002g0145others(49): Show | 52 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.369+1064delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46216383 | |||||
| chr22:46216396
|
A | G | 17 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(14): Show | 17 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.369+1063A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216396 | ||||||
| chr22:46216410
|
A | G | 30 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0006g0029others(27): Show | 30 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.369+1077A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216410 | ||||||
| chr22:46216750
|
A | G | 2 | a0001c0001t0029g0003a0001c0001t0029g0162 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.369+1417A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216750 | ||||||
| chr22:46216775
|
T | C | 65 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(62): Show | 65 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.369+1442T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216775 | ||||||
| chr22:46216800
|
G | C | 1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.370-1463G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216800 | ||||||
| chr22:46216812
|
G | A | 1 | a0001c0001t0010g0040 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.370-1451G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216812 | ||||||
| chr22:46216818
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.370-1445A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46216818 | ||||||
| chr22:46217007
|
C | G | 23 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(20): Show | 23 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.370-1256C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217007 | ||||||
| chr22:46217149
|
C | T | 1 | a0001c0001t0026g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.370-1114C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217149 | ||||||
| chr22:46217199
|
C | T | 1 | a0001c0001t0009g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.370-1064C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217199 | ||||||
| chr22:46217246
|
G | A | 2 | a0001c0001t0020g0178a0001c0001t0057g0157 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.370-1017G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217246 | ||||||
| chr22:46217257
|
A | T | 22 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(19): Show | 22 | HG01109.hp1 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.370-1006A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217257 | ||||||
| chr22:46217340
|
T | A | 89 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(86): Show | 89 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.370-923T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217340 | ||||||
| chr22:46217369
|
C | T | 7 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0015g0136others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-894C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217369 | ||||||
| chr22:46217397
|
G | A | 2 | a0001c0006t0026g0142a0001c0006t0032g0132 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.370-866G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217397 | ||||||
| chr22:46217504
|
C | T | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-759C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217504 | ||||||
| chr22:46217580
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.370-683T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217580 | ||||||
| chr22:46217717
|
G | T | 1 | a0003c0003t0010g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.370-546G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217717 | ||||||
| chr22:46217721
|
G | T | 1 | a0001c0001t0002g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.370-542G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217721 | ||||||
| chr22:46217815
|
C | G | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.370-448C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217815 | ||||||
| chr22:46217819
|
C | CT | 22 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0071others(19): Show | 23 | HG01071.hp1 HG01169.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.370-415dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217819
|
C | CTT | 13 | a0001c0001t0001g0193a0001c0001t0003g0124a0001c0001t0004g0037others(10): Show | 13 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.370-416_370-415dup others(2): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217819
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0003g0101a0001c0001t0003g0144a0001c0001t0012g0083others(3): Show | 6 | HG01891.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-424_370-415dup others(10): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217819
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0006g0143a0001c0001t0039g0041 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.370-425_370-415dup others(11): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217819
|
CT | C | 8 | a0001c0001t0004g0038a0001c0001t0016g0027a0001c0001t0017g0100others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-415delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217819
|
CTT | C | 12 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(9): Show | 12 | HG02451.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.370-416_370-415del others(2): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217819
|
CTTT | C | 10 | a0001c0001t0028g0118a0001c0001t0029g0003a0001c0001t0029g0162others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.370-417_370-415del others(3): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217819
|
CTTTTTTT others(2): Show |
C | 33 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(30): Show | 33 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.370-423_370-415del others(9): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217819
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0002g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.370-433_370-415del others(19): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 46217819 | |||||
| chr22:46217825
|
T | C | 2 | a0001c0001t0020g0178a0001c0001t0057g0157 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.370-438T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217825 | ||||||
| chr22:46217832
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.370-431T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217832 | ||||||
| chr22:46217901
|
G | A | 32 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(29): Show | 32 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.370-362G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217901 | ||||||
| chr22:46217955
|
T | C | 66 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(63): Show | 66 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.370-308T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217955 | ||||||
| chr22:46217965
|
G | T | 3 | a0001c0001t0004g0037a0001c0001t0014g0048a0001c0001t0014g0077 | 3 | HG01884.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.370-298G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46217965 | ||||||
| chr22:46218027
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.370-236C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46218027 | ||||||
| chr22:46218072
|
C | T | 1 | a0001c0001t0019g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.370-191C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46218072 | ||||||
| chr22:46218083
|
A | G | 65 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0095others(62): Show | 65 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.370-180A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46218083 | ||||||
| chr22:46218240
|
TCC | T | 3 | a0001c0001t0002g0189a0001c0001t0002g0191a0001c0001t0012g0137 | 3 | HG03471.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.370-22_370-21delCC | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46218240 | ||||||
| chr22:46218250
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0054g0089 | 2 | HG02145.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.370-13A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 5/8 | chr22 | 46218250 | ||||||
| chr22:46218496
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0004g0038a0001c0001t0015g0136others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+95C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46218496 | ||||||
| chr22:46218572
|
G | A | 1 | a0001c0001t0023g0176 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.508+171G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46218572 | ||||||
| chr22:46218669
|
A | C | 2 | a0001c0001t0004g0049a0001c0001t0004g0060 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+268A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46218669 | ||||||
| chr22:46218835
|
C | CAA | 10 | a0001c0001t0001g0125a0001c0001t0006g0029a0001c0001t0006g0106others(7): Show | 10 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.508+447_508+448dup others(2): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 46218835 | |||||
| chr22:46218846
|
AAAAGAAA others(3): Show |
A | 9 | a0001c0001t0020g0128a0001c0001t0020g0178a0001c0001t0029g0003others(6): Show | 9 | HG02145.hp2 HG02572.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.508+453_508+462del others(10): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 46218846 | |||||
| chr22:46218847
|
AAAGAAAA others(2): Show |
A | 22 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(19): Show | 22 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.508+449_508+457del others(9): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 46218847 | |||||
| chr22:46218856
|
G | A | 41 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0002g0098others(38): Show | 41 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.508+455G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46218856 | ||||||
| chr22:46218993
|
C | A | 8 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.508+592C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46218993 | ||||||
| chr22:46219156
|
C | T | 1 | a0001c0001t0067g0022 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509-656C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46219156 | ||||||
| chr22:46219247
|
G | A | 28 | a0001c0001t0001g0090a0001c0001t0002g0098a0001c0001t0002g0145others(25): Show | 28 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.509-565G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46219247 | ||||||
| chr22:46219479
|
G | A | 9 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(6): Show | 9 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-333G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46219479 | ||||||
| chr22:46219590
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0054g0089 | 2 | HG02145.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.509-222T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46219590 | ||||||
| chr22:46219728
|
G | A | 21 | a0001c0001t0001g0073a0001c0001t0002g0063a0001c0001t0002g0104others(18): Show | 21 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.509-84G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46219728 | ||||||
| chr22:46219745
|
C | T | 12 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0144others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.509-67C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 6/8 | chr22 | 46219745 | ||||||
| chr22:46220140
|
C | T | 1 | a0001c0001t0005g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.711+126C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46220140 | ||||||
| chr22:46220161
|
C | T | 6 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0103others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+147C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46220161 | ||||||
| chr22:46220220
|
A | C | 29 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(26): Show | 29 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.711+206A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46220220 | ||||||
| chr22:46220644
|
T | TA | 6 | a0001c0001t0002g0082a0001c0001t0002g0098a0001c0001t0004g0051others(3): Show | 6 | HG00597.hp1 HG01943.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.711+643dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46220644 | |||||
| chr22:46220835
|
T | C | 127 | a0001c0001t0001g0015a0001c0001t0001g0073a0001c0001t0001g0080others(124): Show | 127 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.711+821T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46220835 | ||||||
| chr22:46220836
|
G | A | 1 | a0001c0001t0016g0027 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.711+822G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46220836 | ||||||
| chr22:46220885
|
G | A | 12 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(9): Show | 12 | HG01433.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.711+871G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46220885 | ||||||
| chr22:46220929
|
C | T | 3 | a0001c0001t0020g0128a0001c0001t0020g0178a0001c0001t0057g0157 | 3 | HG02572.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.711+915C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46220929 | ||||||
| chr22:46220942
|
C | CA | 73 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0002g0098others(70): Show | 74 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.711+938dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46220942 | |||||
| chr22:46220998
|
A | G | 3 | a0001c0001t0058g0079a0001c0001t0073g0042a0001c0001t0074g0112 | 3 | HG02895.hp1 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.711+984A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46220998 | ||||||
| chr22:46221017
|
C | T | 47 | a0001c0001t0001g0125a0001c0001t0003g0124a0001c0001t0004g0037others(44): Show | 47 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(44): Show |
intron_variant | MODIFIER | c.711+1003C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46221017 | ||||||
| chr22:46221061
|
CA | C | 72 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0002g0098others(69): Show | 72 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.711+1049delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46221061 | |||||
| chr22:46221524
|
G | T | 3 | a0001c0001t0026g0152a0001c0006t0026g0142a0001c0006t0032g0132 | 3 | HG01891.hp1 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.711+1510G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46221524 | ||||||
| chr22:46221526
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.711+1512G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46221526 | ||||||
| chr22:46221879
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.711+1865C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46221879 | ||||||
| chr22:46222067
|
ACT | A | 3 | a0001c0001t0020g0128a0001c0001t0020g0178a0001c0001t0057g0157 | 3 | HG02572.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.711+2056_711+2057d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46222067 | |||||
| chr22:46222076
|
C | CA | 8 | a0001c0001t0004g0051a0001c0001t0004g0151a0001c0001t0004g0169others(5): Show | 8 | HG01433.hp2 HG01496.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.711+2073dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46222076 | |||||
| chr22:46222329
|
T | G | 1 | a0001c0001t0045g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.711+2315T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46222329 | ||||||
| chr22:46222454
|
C | G | 1 | a0001c0001t0010g0040 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.711+2440C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46222454 | ||||||
| chr22:46222739
|
G | T | 2 | a0001c0001t0006g0029a0001c0001t0033g0133 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.711+2725G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46222739 | ||||||
| chr22:46222749
|
G | C | 9 | a0001c0001t0006g0143a0001c0001t0012g0083a0001c0001t0014g0046others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+2735G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46222749 | ||||||
| chr22:46223297
|
G | T | 3 | a0001c0001t0026g0152a0001c0001t0073g0042a0001c0001t0074g0112 | 3 | HG02109.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.711+3283G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223297 | ||||||
| chr22:46223303
|
T | C | 25 | a0001c0001t0006g0143a0001c0001t0012g0083a0001c0001t0014g0046others(22): Show | 25 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.711+3289T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223303 | ||||||
| chr22:46223319
|
C | T | 1 | a0001c0001t0023g0081 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.711+3305C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223319 | ||||||
| chr22:46223345
|
A | T | 1 | a0003c0003t0010g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.711+3331A>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223345 | ||||||
| chr22:46223479
|
CTA | C | 3 | a0001c0001t0026g0152a0001c0001t0073g0042a0001c0001t0074g0112 | 3 | HG02109.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.711+3466_711+3467d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223479 | ||||||
| chr22:46223522
|
A | G | 35 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0002g0145others(32): Show | 35 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.711+3508A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223522 | ||||||
| chr22:46223642
|
C | CA | 13 | a0001c0001t0001g0053a0001c0001t0001g0110a0001c0001t0003g0021others(10): Show | 13 | HG01358.hp2 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.711+3644dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46223642 | |||||
| chr22:46223642
|
CA | C | 42 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0002g0098others(39): Show | 42 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.711+3644delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46223642 | |||||
| chr22:46223671
|
T | A | 3 | a0001c0001t0020g0128a0001c0001t0020g0178a0001c0001t0057g0157 | 3 | HG02572.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.711+3657T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223671 | ||||||
| chr22:46223748
|
G | A | 1 | a0001c0001t0015g0123 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.711+3734G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223748 | ||||||
| chr22:46223864
|
G | T | 1 | a0001c0001t0058g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.711+3850G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223864 | ||||||
| chr22:46223899
|
G | A | 1 | a0001c0001t0063g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.711+3885G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223899 | ||||||
| chr22:46223910
|
G | A | 39 | a0001c0001t0003g0124a0001c0001t0004g0037a0001c0001t0004g0051others(36): Show | 39 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.711+3896G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223910 | ||||||
| chr22:46223973
|
T | G | 32 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0002g0145others(29): Show | 32 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.711+3959T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46223973 | ||||||
| chr22:46224034
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0002g0075a0001c0001t0054g0089 | 3 | HG00597.hp2 HG02145.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.711+4020G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46224034 | ||||||
| chr22:46224066
|
C | T | 2 | a0001c0006t0026g0142a0001c0006t0032g0132 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.711+4052C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46224066 | ||||||
| chr22:46224482
|
C | T | 11 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0103others(8): Show | 11 | HG02055.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.711+4468C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46224482 | ||||||
| chr22:46224519
|
G | C | 72 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0002g0098others(69): Show | 72 | HG00639.hp1 HG01069.hp1 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.711+4505G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46224519 | ||||||
| chr22:46224521
|
G | A | 1 | a0001c0001t0061g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.711+4507G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46224521 | ||||||
| chr22:46224804
|
G | A | 20 | a0001c0001t0002g0098a0001c0001t0003g0021a0001c0001t0003g0025others(17): Show | 20 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.711+4790G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46224804 | ||||||
| chr22:46224854
|
C | T | 1 | a0001c0001t0019g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.711+4840C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46224854 | ||||||
| chr22:46224971
|
TG | T | 167 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.711+4966delG | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46224971 | |||||
| chr22:46224976
|
G | T | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.711+4962G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46224976 | ||||||
| chr22:46225148
|
A | G | 88 | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0001g0073others(85): Show | 88 | HG00597.hp1 HG00639.hp1 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.711+5134A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225148 | ||||||
| chr22:46225153
|
G | T | 5 | a0001c0001t0004g0038a0001c0001t0015g0019a0001c0001t0015g0123others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+5139G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225153 | ||||||
| chr22:46225170
|
A | G | 6 | a0001c0001t0004g0051a0001c0001t0004g0151a0001c0001t0004g0172others(3): Show | 6 | HG01943.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.711+5156A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225170 | ||||||
| chr22:46225413
|
G | A | 4 | a0001c0001t0006g0143a0001c0001t0012g0083a0001c0001t0038g0126others(1): Show | 4 | HG01243.hp1 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+5399G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225413 | ||||||
| chr22:46225454
|
G | A | 2 | a0001c0001t0019g0088a0001c0001t0019g0141 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.711+5440G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225454 | ||||||
| chr22:46225490
|
C | T | 8 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0103others(5): Show | 8 | HG02055.hp2 HG02559.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.711+5476C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225490 | ||||||
| chr22:46225576
|
T | C | 5 | a0001c0001t0020g0128a0001c0001t0020g0178a0001c0001t0027g0002others(2): Show | 5 | HG01496.hp2 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+5562T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225576 | ||||||
| chr22:46225749
|
ACACT | A | 10 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(7): Show | 10 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+5739_711+5742d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46225749 | |||||
| chr22:46225776
|
TAA | T | 89 | a0001c0001t0001g0125a0001c0001t0003g0021a0001c0001t0003g0025others(86): Show | 89 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(86): Show |
intron_variant | MODIFIER | c.711+5764_711+5765d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46225776 | |||||
| chr22:46225778
|
A | C | 3 | a0001c0001t0015g0019a0001c0001t0015g0123a0001c0001t0015g0136 | 3 | HG02257.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.711+5764A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225778 | ||||||
| chr22:46225789
|
C | A | 83 | a0001c0001t0001g0125a0001c0001t0003g0021a0001c0001t0003g0025others(80): Show | 83 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.711+5775C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225789 | ||||||
| chr22:46225820
|
C | T | 14 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.711+5806C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225820 | ||||||
| chr22:46225841
|
A | C | 14 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.711+5827A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225841 | ||||||
| chr22:46225846
|
C | T | 3 | a0001c0001t0008g0109a0001c0001t0008g0167a0001c0001t0008g0183 | 3 | HG02109.hp2 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.711+5832C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225846 | ||||||
| chr22:46225854
|
C | A | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.711+5840C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46225854 | ||||||
| chr22:46225992
|
T | TAC | 94 | a0001c0001t0001g0125a0001c0001t0003g0021a0001c0001t0003g0025others(91): Show | 94 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(91): Show |
intron_variant | MODIFIER | c.712-5792_712-5791d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46225992 | |||||
| chr22:46226055
|
CAT | C | 16 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(13): Show | 16 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.712-5736_712-5735d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226055 | ||||||
| chr22:46226097
|
T | C | 114 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0080others(111): Show | 114 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.712-5695T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226097 | ||||||
| chr22:46226117
|
A | G | 29 | a0001c0001t0001g0125a0001c0001t0004g0037a0001c0001t0004g0038others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.712-5675A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226117 | ||||||
| chr22:46226158
|
C | CAT | 4 | a0001c0001t0001g0015a0001c0001t0019g0088a0001c0001t0019g0141others(1): Show | 4 | HG01109.hp2 HG01358.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-5622_712-5621d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46226158 | |||||
| chr22:46226158
|
CAT | C | 91 | a0001c0001t0001g0125a0001c0001t0003g0021a0001c0001t0003g0025others(88): Show | 91 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.712-5622_712-5621d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46226158 | |||||
| chr22:46226160
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.712-5632T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226160 | ||||||
| chr22:46226170
|
T | C | 2 | a0001c0001t0027g0002a0001c0001t0027g0156 | 2 | HG01496.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712-5622T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226170 | ||||||
| chr22:46226231
|
A | G | 10 | a0001c0001t0007g0135a0001c0001t0012g0005a0001c0001t0012g0083others(7): Show | 10 | HG01884.hp2 HG02486.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-5561A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226231 | ||||||
| chr22:46226487
|
T | G | 94 | a0001c0001t0001g0125a0001c0001t0003g0021a0001c0001t0003g0025others(91): Show | 94 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(91): Show |
intron_variant | MODIFIER | c.712-5305T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226487 | ||||||
| chr22:46226517
|
A | C | 4 | a0001c0001t0004g0049a0001c0001t0004g0060a0001c0001t0004g0169others(1): Show | 4 | HG01433.hp2 HG02559.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-5275A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226517 | ||||||
| chr22:46226669
|
A | G | 24 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(21): Show | 24 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.712-5123A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226669 | ||||||
| chr22:46226703
|
T | C | 32 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(29): Show | 32 | HG00639.hp1 HG01243.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.712-5089T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226703 | ||||||
| chr22:46226765
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.712-5027C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226765 | ||||||
| chr22:46226891
|
A | C | 28 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(25): Show | 28 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.712-4901A>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226891 | ||||||
| chr22:46226991
|
C | T | 68 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(65): Show | 68 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.712-4801C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46226991 | ||||||
| chr22:46227087
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.712-4705G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227087 | ||||||
| chr22:46227138
|
A | AATGTGCT others(301): Show |
7 | a0001c0001t0010g0182a0001c0001t0016g0027a0001c0001t0058g0079others(4): Show | 7 | HG00639.hp1 HG01433.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-4638_712-4637i others(310): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46227138 | |||||
| chr22:46227138
|
A | AATGTGCT others(301): Show |
11 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(8): Show | 11 | HG01243.hp1 HG02451.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.712-4638_712-4637i others(310): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46227138 | |||||
| chr22:46227138
|
A | AATGTGCT others(302): Show |
4 | a0001c0001t0010g0040a0001c0001t0016g0160a0001c0001t0016g0194others(1): Show | 4 | HG01884.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-4638_712-4637i others(311): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46227138 | |||||
| chr22:46227138
|
A | AATGTGCT others(302): Show |
5 | a0001c0001t0014g0046a0001c0001t0014g0048a0001c0001t0014g0077others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-4638_712-4637i others(311): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46227138 | |||||
| chr22:46227138
|
A | AATGTGCT others(303): Show |
1 | a0001c0001t0063g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.712-4638_712-4637i others(312): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46227138 | |||||
| chr22:46227185
|
T | C | 1 | a0001c0001t0029g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.712-4607T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227185 | ||||||
| chr22:46227313
|
G | A | 1 | a0001c0001t0054g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.712-4479G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227313 | ||||||
| chr22:46227339
|
C | G | 29 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.712-4453C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227339 | ||||||
| chr22:46227340
|
C | G | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.712-4452C>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227340 | ||||||
| chr22:46227459
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.712-4333C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227459 | ||||||
| chr22:46227544
|
G | A | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.712-4248G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227544 | ||||||
| chr22:46227549
|
G | A | 5 | a0001c0001t0012g0005a0001c0001t0012g0083a0001c0001t0012g0137others(2): Show | 5 | HG02486.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-4243G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227549 | ||||||
| chr22:46227640
|
T | C | 29 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.712-4152T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46227640 | ||||||
| chr22:46228008
|
C | T | 39 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(36): Show | 39 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.712-3784C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46228008 | ||||||
| chr22:46228216
|
T | G | 11 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.712-3576T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46228216 | ||||||
| chr22:46228264
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.712-3528G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46228264 | ||||||
| chr22:46228272
|
C | T | 14 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.712-3520C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46228272 | ||||||
| chr22:46228389
|
A | G | 7 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-3403A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46228389 | ||||||
| chr22:46228399
|
GT | G | 50 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(47): Show | 50 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.712-3391delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46228399 | |||||
| chr22:46228523
|
G | T | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.712-3269G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46228523 | ||||||
| chr22:46228765
|
AT | A | 5 | a0001c0001t0015g0019a0001c0001t0015g0123a0001c0001t0015g0136others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-3025delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46228765 | |||||
| chr22:46228803
|
CA | C | 7 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-2988delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46228803 | ||||||
| chr22:46228948
|
C | CA | 17 | a0001c0001t0002g0098a0001c0001t0003g0147a0001c0001t0007g0020others(14): Show | 17 | HG01109.hp1 HG01943.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.712-2835dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46228948 | |||||
| chr22:46229032
|
G | A | 1 | a0001c0001t0035g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.712-2760G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229032 | ||||||
| chr22:46229084
|
G | A | 1 | a0001c0001t0035g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.712-2708G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229084 | ||||||
| chr22:46229106
|
CA | C | 40 | a0001c0001t0001g0125a0001c0001t0004g0037a0001c0001t0004g0038others(37): Show | 40 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.712-2671delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46229106 | |||||
| chr22:46229106
|
CAA | C | 40 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(37): Show | 40 | HG00639.hp1 HG01243.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.712-2672_712-2671d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46229106 | |||||
| chr22:46229106
|
CAAA | C | 13 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.712-2673_712-2671d others(5): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46229106 | |||||
| chr22:46229236
|
C | A | 2 | a0001c0001t0017g0100a0001c0001t0068g0119 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.712-2556C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229236 | ||||||
| chr22:46229291
|
T | C | 1 | a0001c0001t0075g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.712-2501T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229291 | ||||||
| chr22:46229332
|
T | C | 1 | a0001c0001t0025g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.712-2460T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229332 | ||||||
| chr22:46229414
|
G | A | 1 | a0001c0001t0025g0056 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.712-2378G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229414 | ||||||
| chr22:46229443
|
C | T | 2 | a0001c0001t0019g0088a0001c0001t0019g0141 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.712-2349C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229443 | ||||||
| chr22:46229534
|
G | T | 1 | a0001c0001t0069g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.712-2258G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229534 | ||||||
| chr22:46229558
|
C | CA | 17 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(14): Show | 17 | HG00438.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.712-2219dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46229558 | |||||
| chr22:46229682
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.712-2110G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229682 | ||||||
| chr22:46229911
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.712-1881C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46229911 | ||||||
| chr22:46230097
|
C | T | 4 | a0001c0001t0014g0046a0001c0001t0014g0048a0001c0001t0014g0077others(1): Show | 4 | HG01884.hp2 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-1695C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46230097 | ||||||
| chr22:46230099
|
C | T | 3 | a0001c0001t0015g0019a0001c0001t0015g0123a0001c0001t0015g0136 | 3 | HG02257.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.712-1693C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46230099 | ||||||
| chr22:46230193
|
G | A | 29 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.712-1599G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46230193 | ||||||
| chr22:46230371
|
C | CA | 58 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(55): Show | 58 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.712-1411dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46230371 | |||||
| chr22:46230371
|
C | CAA | 31 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(28): Show | 31 | HG00639.hp1 HG01243.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.712-1412_712-1411d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46230371 | |||||
| chr22:46230402
|
T | C | 1 | a0001c0001t0016g0160 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.712-1390T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46230402 | ||||||
| chr22:46230535
|
C | T | 64 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(61): Show | 64 | HG00639.hp1 HG01109.hp1 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.712-1257C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46230535 | ||||||
| chr22:46230609
|
G | A | 66 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(63): Show | 66 | HG00639.hp1 HG01109.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.712-1183G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46230609 | ||||||
| chr22:46230817
|
C | T | 14 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.712-975C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46230817 | ||||||
| chr22:46231120
|
G | A | 1 | a0001c0001t0035g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.712-672G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231120 | ||||||
| chr22:46231220
|
A | ATT | 7 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-557_712-556dup others(2): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 46231220 | |||||
| chr22:46231241
|
C | T | 3 | a0001c0001t0015g0019a0001c0001t0015g0123a0001c0001t0015g0136 | 3 | HG02257.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.712-551C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231241 | ||||||
| chr22:46231250
|
G | A | 1 | a0004c0008t0009g0146 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.712-542G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231250 | ||||||
| chr22:46231279
|
C | T | 29 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.712-513C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231279 | ||||||
| chr22:46231280
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.712-512G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231280 | ||||||
| chr22:46231285
|
G | C | 93 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(90): Show | 93 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(90): Show |
intron_variant | MODIFIER | c.712-507G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231285 | ||||||
| chr22:46231343
|
C | A | 7 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-449C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231343 | ||||||
| chr22:46231501
|
G | A | 7 | a0001c0001t0001g0072a0001c0001t0001g0080a0001c0001t0001g0095others(4): Show | 7 | HG00438.hp2 HG01496.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.712-291G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231501 | ||||||
| chr22:46231641
|
T | G | 1 | a0001c0001t0078g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.712-151T>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231641 | ||||||
| chr22:46231661
|
G | A | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.712-131G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231661 | ||||||
| chr22:46231706
|
C | T | 7 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-86C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 7/8 | chr22 | 46231706 | ||||||
| chr22:46232387
|
G | A | 2 | a0001c0001t0019g0088a0001c0001t0019g0141 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1159+148G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46232387 | ||||||
| chr22:46232812
|
C | CA | 16 | a0001c0001t0001g0139a0001c0001t0004g0037a0001c0001t0004g0038others(13): Show | 16 | HG00738.hp1 HG01069.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1159+584dupA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 46232812 | |||||
| chr22:46232961
|
G | A | 15 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0120others(12): Show | 15 | HG01109.hp1 HG01943.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1159+722G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46232961 | ||||||
| chr22:46232981
|
CA | C | 80 | a0001c0001t0002g0117a0001c0001t0003g0021a0001c0001t0003g0025others(77): Show | 80 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(77): Show |
intron_variant | MODIFIER | c.1159+762delA | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 46232981 | |||||
| chr22:46232981
|
CAA | C | 12 | a0001c0001t0005g0009a0001c0001t0007g0121a0001c0001t0012g0005others(9): Show | 12 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1159+761_1159+762d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 46232981 | |||||
| chr22:46233005
|
TAC | T | 65 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0101others(62): Show | 65 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.1159+786_1159+787d others(4): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 46233005 | |||||
| chr22:46233005
|
TACAC | T | 14 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1159+784_1159+787d others(6): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 46233005 | |||||
| chr22:46233063
|
T | C | 9 | a0001c0001t0006g0029a0001c0001t0006g0106a0001c0001t0006g0134others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1159+824T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233063 | ||||||
| chr22:46233095
|
T | C | 29 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(26): Show | 29 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1159+856T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233095 | ||||||
| chr22:46233206
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1159+967T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233206 | ||||||
| chr22:46233523
|
C | T | 1 | a0001c0001t0007g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1159+1284C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233523 | ||||||
| chr22:46233574
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1159+1335G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233574 | ||||||
| chr22:46233582
|
A | G | 51 | a0001c0001t0001g0125a0001c0001t0004g0037a0001c0001t0004g0038others(48): Show | 51 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.1159+1343A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233582 | ||||||
| chr22:46233602
|
G | A | 1 | a0001c0006t0026g0142 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1159+1363G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233602 | ||||||
| chr22:46233716
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1160-1417T>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233716 | ||||||
| chr22:46233827
|
C | CT | 15 | a0001c0001t0001g0057a0001c0001t0002g0065a0001c0001t0009g0173others(12): Show | 15 | HG00639.hp1 HG00639.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1160-1292dupT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 46233827 | |||||
| chr22:46233827
|
CT | C | 6 | a0001c0001t0004g0038a0001c0001t0018g0097a0001c0001t0018g0186others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-1292delT | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr22 | 46233827 | |||||
| chr22:46233849
|
A | G | 1 | a0001c0001t0013g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1160-1284A>G | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46233849 | ||||||
| chr22:46234055
|
C | T | 3 | a0001c0001t0077g0004a0001c0001t0078g0196a0001c0001t0079g0107 | 3 | HG02258.hp2 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1160-1078C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234055 | ||||||
| chr22:46234113
|
T | C | 2 | a0001c0001t0073g0042a0001c0001t0074g0112 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1160-1020T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234113 | ||||||
| chr22:46234188
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1160-945G>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234188 | ||||||
| chr22:46234361
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0002g0117 | 2 | NA18945.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1160-772T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234361 | ||||||
| chr22:46234634
|
C | T | 1 | a0001c0001t0014g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1160-499C>T | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234634 | ||||||
| chr22:46234647
|
C | A | 7 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0011others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160-486C>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234647 | ||||||
| chr22:46234725
|
G | A | 34 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0049others(31): Show | 34 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.1160-408G>A | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234725 | ||||||
| chr22:46234737
|
G | C | 94 | a0001c0001t0002g0191a0001c0001t0003g0021a0001c0001t0003g0025others(91): Show | 94 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(91): Show |
intron_variant | MODIFIER | c.1160-396G>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234737 | ||||||
| chr22:46234896
|
T | C | 5 | a0001c0001t0012g0005a0001c0001t0012g0083a0001c0001t0012g0137others(2): Show | 5 | HG02486.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-237T>C | PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 8/8 | chr22 | 46234896 |