Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 133522 |
| ensemblid | ENSG00000155846.17 |
| hgncid | 30022 |
| symbol | PPARGC1B |
| name | PPARG coactivator 1 beta |
| refseq_nuc | NM_133263.4 |
| refseq_prot | NP_573570.3 |
| ensembl_nuc | ENST00000309241.10 |
| ensembl_prot | ENSP00000312649.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 149730310 |
| end | 149855022 |
| strand | + |
| ver | v1.2 |
| region | chr5:149730310-149855022 |
| region5000 | chr5:149725310-149860022 |
| regionname0 | PPARGC1B_chr5_149730310_149855022 |
| regionname5000 | PPARGC1B_chr5_149725310_149860022 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1023 | 192 | 37 | 36 | 81 | 9 | 27 | 60 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0002 | 0/0 | 1023 | 41 | 19 | 4 | 15 | 0 | 3 | 12 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0003 | 0/0 | 1023 | 30 | 0 | 13 | 15 | 1 | 1 | 13 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0004 | 0/0 | 1023 | 24 | 8 | 6 | 7 | 0 | 3 | 5 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0005 | 0/0 | 1023 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0006 | 0/0 | 1023 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0007 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0008 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0009 | 0/0 | 1023 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0010 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0011 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0012 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0013 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0014 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0015 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0016 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| a0017 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | MAGND others(1018): Show |
chr5 | 149725310 | 149860022 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3069 | 142 | 12 | 28 | 76 | 6 | 18 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0004 | 0/0 | 3069 | 21 | 7 | 3 | 4 | 2 | 5 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0006 | 0/0 | 3069 | 7 | 6 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0009 | 0/0 | 3069 | 6 | 3 | 2 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0010 | 0/0 | 3069 | 6 | 6 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0017 | 0/0 | 3069 | 3 | 2 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0018 | 0/0 | 3069 | 3 | 0 | 2 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0022 | 0/0 | 3069 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0024 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0030 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0001c0033 | 0/0 | 3069 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0002c0002 | 0/0 | 3069 | 31 | 13 | 4 | 12 | 0 | 2 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0002c0008 | 0/0 | 3069 | 6 | 6 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0002c0014 | 0/0 | 3069 | 4 | 0 | 0 | 3 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0003c0003 | 0/0 | 3069 | 25 | 0 | 13 | 10 | 1 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0003c0012 | 0/0 | 3069 | 5 | 0 | 0 | 5 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0004c0005 | 0/0 | 3069 | 21 | 5 | 6 | 7 | 0 | 3 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0004c0015 | 0/0 | 3069 | 3 | 3 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0005c0011 | 0/0 | 3069 | 5 | 3 | 2 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0005c0013 | 0/0 | 3069 | 4 | 4 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0005c0026 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0006c0007 | 0/0 | 3069 | 7 | 7 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0007c0019 | 0/0 | 3069 | 2 | 2 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0007c0023 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0008c0016 | 0/0 | 3069 | 3 | 3 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0009c0020 | 0/0 | 3069 | 2 | 2 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0010c0021 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0011c0028 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0012c0031 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0013c0027 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0014c0025 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0015c0029 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0016c0032 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 | ||
| a0017c0034 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | ATGGC others(3064): Show |
chr5 | 149725310 | 149860022 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 10569 | 43 | 6 | 9 | 22 | 1 | 4 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0002 | 1/0 | 10569 | 27 | 0 | 8 | 11 | 2 | 5 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0003 | 0/0 | 10569 | 23 | 0 | 2 | 17 | 1 | 3 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0007 | 0/0 | 10569 | 9 | 0 | 0 | 9 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0009 | 0/0 | 10570 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0012 | 0/0 | 10569 | 6 | 0 | 0 | 6 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0015 | 0/0 | 10568 | 5 | 0 | 0 | 4 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0019 | 0/0 | 10569 | 4 | 0 | 2 | 0 | 1 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0020 | 0/0 | 10568 | 3 | 0 | 1 | 2 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0021 | 0/0 | 10569 | 3 | 1 | 2 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0023 | 0/0 | 10568 | 2 | 0 | 0 | 1 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0028 | 0/0 | 10569 | 2 | 1 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0039 | 0/0 | 10569 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0040 | 0/0 | 10569 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0041 | 0/0 | 10569 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0043 | 0/0 | 10569 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0044 | 0/0 | 10568 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0045 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0047 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0048 | 0/0 | 10568 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0050 | 0/0 | 10569 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0051 | 0/0 | 10569 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0053 | 0/0 | 10569 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0054 | 0/0 | 10569 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0057 | 0/0 | 10569 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0001t0070 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0004t0006 | 0/0 | 10572 | 11 | 0 | 2 | 4 | 0 | 5 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10567): Show |
chr5 | 149725310 | 149860022 |
| a0001c0004t0018 | 0/0 | 10572 | 4 | 4 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10567): Show |
chr5 | 149725310 | 149860022 |
| a0001c0004t0024 | 0/0 | 10569 | 3 | 3 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0004t0030 | 0/0 | 10569 | 2 | 0 | 1 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0004t0062 | 0/0 | 10572 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10567): Show |
chr5 | 149725310 | 149860022 |
| a0001c0006t0001 | 0/0 | 10569 | 6 | 6 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0006t0042 | 0/0 | 10569 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0009t0002 | 0/0 | 10569 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0009t0009 | 0/0 | 10570 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0001c0009t0023 | 0/0 | 10568 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0001c0009t0027 | 0/0 | 10569 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0009t0046 | 0/0 | 10568 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0001c0009t0064 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0010t0001 | 0/0 | 10569 | 3 | 3 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0010t0009 | 0/0 | 10570 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0001c0010t0038 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0010t0056 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0017t0006 | 0/0 | 10572 | 2 | 1 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10567): Show |
chr5 | 149725310 | 149860022 |
| a0001c0017t0017 | 0/0 | 10570 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0001c0018t0029 | 0/0 | 10571 | 2 | 0 | 1 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10566): Show |
chr5 | 149725310 | 149860022 |
| a0001c0018t0058 | 0/0 | 10570 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0001c0022t0006 | 0/0 | 10572 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10567): Show |
chr5 | 149725310 | 149860022 |
| a0001c0024t0001 | 0/0 | 10569 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0030t0031 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0001c0033t0001 | 0/0 | 10569 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0005 | 0/0 | 10569 | 11 | 6 | 1 | 4 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0008 | 0/0 | 10569 | 3 | 3 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0010 | 0/0 | 10570 | 8 | 0 | 1 | 6 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0025 | 0/0 | 10569 | 3 | 0 | 2 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0032 | 0/0 | 10568 | 2 | 1 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0065 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0066 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0067 | 0/0 | 10569 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0002t0068 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0008t0005 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0008t0008 | 0/0 | 10569 | 3 | 3 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0008t0063 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0008t0071 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0002c0014t0005 | 0/0 | 10569 | 4 | 0 | 0 | 3 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0003c0003t0004 | 0/0 | 10574 | 16 | 0 | 6 | 8 | 1 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10569): Show |
chr5 | 149725310 | 149860022 |
| a0003c0003t0011 | 0/0 | 10573 | 6 | 0 | 6 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10568): Show |
chr5 | 149725310 | 149860022 |
| a0003c0003t0033 | 0/0 | 10573 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10568): Show |
chr5 | 149725310 | 149860022 |
| a0003c0003t0035 | 0/0 | 10573 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10568): Show |
chr5 | 149725310 | 149860022 |
| a0003c0003t0052 | 0/0 | 10573 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10568): Show |
chr5 | 149725310 | 149860022 |
| a0003c0012t0014 | 0/0 | 10574 | 5 | 0 | 0 | 5 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10569): Show |
chr5 | 149725310 | 149860022 |
| a0004c0005t0001 | 0/0 | 10569 | 10 | 2 | 5 | 2 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0004c0005t0012 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0004c0005t0013 | 0/0 | 10569 | 5 | 2 | 1 | 1 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0004c0005t0022 | 0/0 | 10569 | 3 | 0 | 0 | 3 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0004c0005t0049 | 0/0 | 10568 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0004c0005t0055 | 0/0 | 10569 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0004c0015t0001 | 0/0 | 10569 | 3 | 3 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0005c0011t0001 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0005c0011t0009 | 0/0 | 10570 | 3 | 1 | 2 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0005c0011t0027 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0005c0013t0001 | 0/0 | 10569 | 2 | 2 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0005c0013t0009 | 0/0 | 10570 | 2 | 2 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0005c0026t0034 | 0/0 | 10570 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0006c0007t0016 | 0/0 | 10569 | 5 | 5 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0006c0007t0059 | 0/0 | 10568 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10563): Show |
chr5 | 149725310 | 149860022 |
| a0006c0007t0060 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0007c0019t0017 | 0/0 | 10570 | 2 | 2 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0007c0023t0017 | 0/0 | 10570 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10565): Show |
chr5 | 149725310 | 149860022 |
| a0008c0016t0026 | 0/0 | 10574 | 2 | 2 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10569): Show |
chr5 | 149725310 | 149860022 |
| a0008c0016t0036 | 0/0 | 10573 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10568): Show |
chr5 | 149725310 | 149860022 |
| a0009c0020t0008 | 0/0 | 10569 | 2 | 2 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0010c0021t0061 | 0/0 | 10571 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10566): Show |
chr5 | 149725310 | 149860022 |
| a0011c0028t0011 | 0/0 | 10573 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10568): Show |
chr5 | 149725310 | 149860022 |
| a0012c0031t0002 | 0/0 | 10569 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0013c0027t0037 | 0/0 | 10573 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10568): Show |
chr5 | 149725310 | 149860022 |
| a0014c0025t0031 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0015c0029t0008 | 0/0 | 10569 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0016c0032t0069 | 0/0 | 10569 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| a0017c0034t0013 | 0/0 | 10569 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | GACTC others(10564): Show |
chr5 | 149725310 | 149860022 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0012g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0012g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0012g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0012g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0015g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0015g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0015g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0015g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0015g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0019g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0019g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0019g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0019g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0020g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0020g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0021g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0021g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0021g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0023g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0023g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0028g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0028g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0039g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0040g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0041g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0043g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0044g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0045g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0047g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0048g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0050g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0051g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0053g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0054g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0057g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0001t0070g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0006g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0018g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0018g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0018g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0024g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0024g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0024g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0030g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0030g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0004t0062g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0006t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0006t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0006t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0006t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0006t0042g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0009t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0009t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0009t0023g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0009t0027g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0009t0046g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0009t0064g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0010t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0010t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0010t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0010t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0010t0038g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0010t0056g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0017t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0017t0006g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0017t0017g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0018t0029g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0018t0029g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0018t0058g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0022t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0024t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0030t0031g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0001c0033t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0010g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0010g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0010g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0010g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0010g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0025g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0025g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0025g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0032g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0032g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0065g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0066g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0067g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0002t0068g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0008t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0008t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0008t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0008t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0008t0063g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0008t0071g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0014t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0014t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0014t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0002c0014t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0011g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0011g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0011g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0011g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0011g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0011g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0033g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0035g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0003t0052g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0012t0014g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0012t0014g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0012t0014g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0012t0014g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0003c0012t0014g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0012g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0013g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0013g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0013g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0013g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0013g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0022g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0022g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0022g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0049g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0005t0055g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0015t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0015t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0004c0015t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0011t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0011t0009g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0011t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0011t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0011t0027g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0013t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0013t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0013t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0013t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0005c0026t0034g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0006c0007t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0006c0007t0016g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0006c0007t0016g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0006c0007t0016g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0006c0007t0016g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0006c0007t0059g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0006c0007t0060g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0007c0019t0017g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0007c0019t0017g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0007c0023t0017g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0008c0016t0026g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0008c0016t0026g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0008c0016t0036g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0009c0020t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0009c0020t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0010c0021t0061g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0011c0028t0011g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0012c0031t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0013c0027t0037g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0014c0025t0031g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0015c0029t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0016c0032t0069g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| a0017c0034t0013g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0019 | g0072 | EUR | GBR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0022 | EUR | GBR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0308 | EUR | GBR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00140 | hp2 | a0003 | c0003 | t0004 | g0306 | EUR | GBR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00280 | hp1 | a0001 | c0018 | t0029 | g0217 | EUR | FIN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00280 | hp2 | a0001 | c0004 | t0030 | g0113 | EUR | FIN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00408 | hp1 | a0001 | c0001 | t0054 | g0223 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00558 | hp1 | a0001 | c0001 | t0015 | g0189 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00609 | hp2 | a0002 | c0014 | t0005 | g0019 | EAS | CHS | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00639 | hp2 | a0004 | c0005 | t0001 | g0257 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00735 | hp2 | a0010 | c0021 | t0061 | g0311 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00738 | hp1 | a0002 | c0002 | t0025 | g0029 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00741 | hp1 | a0001 | c0001 | t0021 | g0140 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG00741 | hp2 | a0001 | c0001 | t0028 | g0224 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01069 | hp1 | a0001 | c0004 | t0030 | g0253 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01069 | hp2 | a0005 | c0011 | t0009 | g0088 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01071 | hp1 | a0005 | c0011 | t0009 | g0054 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01074 | hp2 | a0001 | c0018 | t0058 | g0211 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01106 | hp1 | a0001 | c0001 | t0057 | g0238 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01106 | hp2 | a0004 | c0005 | t0001 | g0139 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01109 | hp1 | a0004 | c0005 | t0001 | g0159 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01109 | hp2 | a0001 | c0001 | t0019 | g0052 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01168 | hp1 | a0001 | c0004 | t0006 | g0102 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01175 | hp1 | a0001 | c0018 | t0029 | g0197 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01243 | hp1 | a0001 | c0009 | t0027 | g0213 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01243 | hp2 | a0002 | c0002 | t0005 | g0059 | AMR | PUR | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01258 | hp1 | a0001 | c0001 | t0021 | g0225 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01258 | hp2 | a0004 | c0005 | t0001 | g0245 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01261 | hp2 | a0002 | c0002 | t0010 | g0066 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01346 | hp2 | a0001 | c0009 | t0002 | g0117 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01361 | hp1 | a0001 | c0001 | t0019 | g0082 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01433 | hp1 | a0003 | c0003 | t0004 | g0295 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01496 | hp1 | a0003 | c0003 | t0004 | g0294 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01496 | hp2 | a0001 | c0006 | t0042 | g0001 | AMR | CLM | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01884 | hp1 | a0004 | c0015 | t0001 | g0196 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01884 | hp2 | a0001 | c0004 | t0024 | g0080 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01891 | hp1 | a0001 | c0001 | t0021 | g0146 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01891 | hp2 | a0002 | c0002 | t0066 | g0079 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01928 | hp1 | a0001 | c0001 | t0043 | g0254 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01928 | hp2 | a0003 | c0003 | t0011 | g0279 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01934 | hp1 | a0003 | c0003 | t0004 | g0309 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01934 | hp2 | a0004 | c0005 | t0001 | g0248 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01943 | hp1 | a0003 | c0003 | t0004 | g0287 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01943 | hp2 | a0001 | c0001 | t0051 | g0145 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01952 | hp1 | a0003 | c0003 | t0011 | g0063 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01975 | hp1 | a0003 | c0003 | t0035 | g0297 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01978 | hp1 | a0003 | c0003 | t0011 | g0303 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01993 | hp1 | a0003 | c0003 | t0011 | g0301 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG01993 | hp2 | a0002 | c0002 | t0025 | g0027 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02004 | hp1 | a0011 | c0028 | t0011 | g0136 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02004 | hp2 | a0012 | c0031 | t0002 | g0235 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02040 | hp2 | a0001 | c0001 | t0015 | g0180 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02056 | hp1 | a0002 | c0002 | t0005 | g0179 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02071 | hp1 | a0003 | c0003 | t0004 | g0177 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02132 | hp2 | a0003 | c0003 | t0004 | g0150 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02135 | hp1 | a0004 | c0005 | t0001 | g0171 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02145 | hp1 | a0002 | c0008 | t0063 | g0169 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02145 | hp2 | a0004 | c0015 | t0001 | g0118 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02148 | hp1 | a0003 | c0003 | t0011 | g0237 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02148 | hp2 | a0003 | c0003 | t0004 | g0293 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CDX | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02155 | hp2 | a0001 | c0001 | t0040 | g0065 | EAS | CDX | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02165 | hp1 | a0002 | c0014 | t0005 | g0260 | EAS | CDX | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02165 | hp2 | a0004 | c0005 | t0049 | g0243 | EAS | CDX | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02257 | hp1 | a0001 | c0001 | t0028 | g0214 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02257 | hp2 | a0007 | c0023 | t0017 | g0108 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02258 | hp1 | a0001 | c0010 | t0001 | g0255 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02258 | hp2 | a0001 | c0004 | t0024 | g0077 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02273 | hp1 | a0001 | c0001 | t0020 | g0137 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02273 | hp2 | a0003 | c0003 | t0004 | g0296 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02280 | hp1 | a0001 | c0004 | t0018 | g0166 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02280 | hp2 | a0004 | c0005 | t0001 | g0011 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02293 | hp1 | a0003 | c0003 | t0011 | g0302 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02293 | hp2 | a0001 | c0004 | t0006 | g0193 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02300 | hp2 | a0004 | c0005 | t0013 | g0239 | AMR | PEL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02451 | hp1 | a0013 | c0027 | t0037 | g0318 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02451 | hp2 | a0009 | c0020 | t0008 | g0005 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | KHV | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02572 | hp1 | a0001 | c0017 | t0017 | g0014 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02572 | hp2 | a0002 | c0002 | t0008 | g0055 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02602 | hp2 | a0001 | c0001 | t0019 | g0089 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02630 | hp1 | a0001 | c0010 | t0056 | g0153 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02630 | hp2 | a0002 | c0002 | t0032 | g0263 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02647 | hp1 | a0008 | c0016 | t0036 | g0122 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02647 | hp2 | a0006 | c0007 | t0016 | g0012 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02683 | hp1 | a0002 | c0002 | t0025 | g0286 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02723 | hp1 | a0001 | c0009 | t0009 | g0130 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02723 | hp2 | a0005 | c0011 | t0027 | g0132 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02735 | hp1 | a0001 | c0001 | t0015 | g0300 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02735 | hp2 | a0001 | c0001 | t0023 | g0229 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02738 | hp1 | a0001 | c0004 | t0006 | g0112 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02809 | hp1 | a0001 | c0004 | t0018 | g0034 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02809 | hp2 | a0002 | c0008 | t0008 | g0319 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02818 | hp1 | a0008 | c0016 | t0026 | g0009 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02818 | hp2 | a0002 | c0008 | t0008 | g0015 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02886 | hp1 | a0002 | c0002 | t0005 | g0212 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02886 | hp2 | a0001 | c0010 | t0038 | g0185 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02895 | hp1 | a0002 | c0008 | t0071 | g0184 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02895 | hp2 | a0002 | c0002 | t0005 | g0267 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02896 | hp1 | a0006 | c0007 | t0059 | g0033 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02896 | hp2 | a0001 | c0001 | t0047 | g0265 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02897 | hp1 | a0002 | c0002 | t0005 | g0266 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02897 | hp2 | a0006 | c0007 | t0016 | g0040 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02922 | hp1 | a0006 | c0007 | t0016 | g0131 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02922 | hp2 | a0002 | c0002 | t0008 | g0003 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02965 | hp1 | a0001 | c0017 | t0006 | g0078 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02965 | hp2 | a0005 | c0026 | t0034 | g0310 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02976 | hp1 | a0001 | c0009 | t0046 | g0042 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02976 | hp2 | a0001 | c0004 | t0018 | g0039 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03017 | hp1 | a0001 | c0001 | t0053 | g0216 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03017 | hp2 | a0001 | c0022 | t0006 | g0097 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03041 | hp1 | a0002 | c0002 | t0065 | g0051 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03041 | hp2 | a0001 | c0030 | t0031 | g0320 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03098 | hp1 | a0005 | c0011 | t0009 | g0133 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0209 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03130 | hp1 | a0001 | c0006 | t0001 | g0313 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03130 | hp2 | a0001 | c0009 | t0064 | g0261 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03139 | hp1 | a0006 | c0007 | t0016 | g0035 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0100 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03195 | hp1 | a0009 | c0020 | t0008 | g0004 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03195 | hp2 | a0005 | c0013 | t0009 | g0008 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0142 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03209 | hp2 | a0005 | c0013 | t0001 | g0317 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03225 | hp1 | a0001 | c0010 | t0001 | g0256 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03225 | hp2 | a0007 | c0019 | t0017 | g0315 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03453 | hp1 | a0001 | c0004 | t0024 | g0037 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03453 | hp2 | a0014 | c0025 | t0031 | g0043 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03486 | hp1 | a0005 | c0013 | t0009 | g0007 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03486 | hp2 | a0008 | c0016 | t0026 | g0262 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03491 | hp1 | a0001 | c0009 | t0023 | g0218 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03491 | hp2 | a0001 | c0001 | t0044 | g0064 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03516 | hp1 | a0001 | c0001 | t0045 | g0198 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03516 | hp2 | a0001 | c0006 | t0001 | g0199 | AFR | ESN | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03540 | hp1 | a0006 | c0007 | t0016 | g0147 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03540 | hp2 | a0001 | c0010 | t0009 | g0036 | AFR | GWD | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03579 | hp2 | a0002 | c0002 | t0008 | g0030 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03669 | hp1 | a0004 | c0005 | t0013 | g0241 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03669 | hp2 | a0004 | c0005 | t0055 | g0086 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03688 | hp1 | a0001 | c0001 | t0041 | g0222 | SAS | STU | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | STU | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03704 | hp2 | a0001 | c0004 | t0006 | g0277 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03710 | hp1 | a0001 | c0017 | t0006 | g0219 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | BEB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03834 | hp1 | a0001 | c0004 | t0006 | g0210 | SAS | BEB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03834 | hp2 | a0003 | c0003 | t0004 | g0288 | SAS | BEB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03942 | hp2 | a0002 | c0014 | t0005 | g0017 | SAS | BEB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG04115 | hp1 | a0001 | c0004 | t0006 | g0095 | SAS | STU | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | STU | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG04184 | hp1 | a0001 | c0004 | t0006 | g0115 | SAS | BEB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG04184 | hp2 | a0002 | c0002 | t0010 | g0304 | SAS | BEB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | STU | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG04199 | hp2 | a0001 | c0033 | t0001 | g0096 | SAS | STU | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18522 | hp1 | a0015 | c0029 | t0008 | g0270 | AFR | YRI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0316 | AFR | YRI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18906 | hp2 | a0005 | c0011 | t0001 | g0128 | AFR | YRI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18941 | hp1 | a0016 | c0032 | t0069 | g0127 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18941 | hp2 | a0002 | c0002 | t0032 | g0041 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18943 | hp2 | a0002 | c0002 | t0010 | g0204 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18944 | hp1 | a0002 | c0002 | t0010 | g0073 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0178 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18948 | hp1 | a0001 | c0001 | t0015 | g0232 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18949 | hp2 | a0004 | c0005 | t0022 | g0234 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18951 | hp2 | a0003 | c0012 | t0014 | g0111 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18952 | hp1 | a0003 | c0012 | t0014 | g0116 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18962 | hp1 | a0001 | c0001 | t0023 | g0203 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18962 | hp2 | a0003 | c0003 | t0004 | g0290 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18963 | hp1 | a0002 | c0002 | t0010 | g0125 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18963 | hp2 | a0001 | c0001 | t0012 | g0124 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18964 | hp1 | a0003 | c0003 | t0033 | g0292 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18964 | hp2 | a0001 | c0001 | t0012 | g0090 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18974 | hp1 | a0001 | c0004 | t0006 | g0107 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18974 | hp2 | a0001 | c0001 | t0020 | g0299 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0215 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18980 | hp2 | a0003 | c0003 | t0004 | g0247 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18981 | hp2 | a0003 | c0012 | t0014 | g0120 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0175 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18984 | hp1 | a0001 | c0001 | t0012 | g0046 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18984 | hp2 | a0001 | c0001 | t0007 | g0188 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18989 | hp1 | a0001 | c0001 | t0012 | g0085 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18989 | hp2 | a0003 | c0012 | t0014 | g0157 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18990 | hp1 | a0004 | c0005 | t0022 | g0109 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18994 | hp1 | a0002 | c0002 | t0010 | g0038 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18994 | hp2 | a0002 | c0002 | t0005 | g0084 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18998 | hp1 | a0001 | c0024 | t0001 | g0091 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18999 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18999 | hp2 | a0001 | c0001 | t0048 | g0049 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19000 | hp1 | a0003 | c0003 | t0004 | g0305 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19004 | hp1 | a0003 | c0003 | t0004 | g0281 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19004 | hp2 | a0001 | c0001 | t0020 | g0126 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19005 | hp1 | a0003 | c0003 | t0004 | g0045 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19005 | hp2 | a0001 | c0001 | t0012 | g0162 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19007 | hp1 | a0017 | c0034 | t0013 | g0021 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19010 | hp1 | a0001 | c0001 | t0012 | g0048 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19012 | hp1 | a0003 | c0003 | t0052 | g0192 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19030 | hp1 | a0001 | c0004 | t0018 | g0031 | AFR | LWK | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | LWK | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19043 | hp1 | a0004 | c0015 | t0001 | g0119 | AFR | LWK | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19055 | hp2 | a0001 | c0001 | t0015 | g0289 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19056 | hp2 | a0002 | c0002 | t0005 | g0168 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19058 | hp2 | a0002 | c0002 | t0010 | g0060 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19066 | hp2 | a0002 | c0014 | t0005 | g0259 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19068 | hp1 | a0004 | c0005 | t0001 | g0246 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19068 | hp2 | a0004 | c0005 | t0013 | g0071 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19070 | hp1 | a0001 | c0004 | t0006 | g0105 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19070 | hp2 | a0002 | c0002 | t0010 | g0264 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19076 | hp2 | a0002 | c0002 | t0005 | g0016 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19079 | hp1 | a0004 | c0005 | t0022 | g0114 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19080 | hp1 | a0001 | c0001 | t0050 | g0202 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19080 | hp2 | a0002 | c0002 | t0067 | g0023 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19081 | hp2 | a0001 | c0004 | t0006 | g0101 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19082 | hp2 | a0001 | c0004 | t0006 | g0104 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19085 | hp1 | a0003 | c0012 | t0014 | g0110 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19088 | hp1 | a0003 | c0003 | t0004 | g0291 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA19240 | hp2 | a0002 | c0008 | t0005 | g0129 | AFR | YRI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20129 | hp1 | a0004 | c0005 | t0001 | g0121 | AFR | ASW | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20129 | hp2 | a0005 | c0013 | t0001 | g0013 | AFR | ASW | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0284 | EUR | TSI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20752 | hp2 | a0001 | c0004 | t0062 | g0252 | EUR | TSI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20805 | hp2 | a0001 | c0001 | t0039 | g0141 | EUR | TSI | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | GIH | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20905 | hp2 | a0004 | c0005 | t0001 | g0251 | SAS | GIH | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02109 | hp2 | a0001 | c0010 | t0001 | g0056 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02486 | hp1 | a0001 | c0001 | t0070 | g0144 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02486 | hp2 | a0002 | c0002 | t0068 | g0250 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02559 | hp1 | a0004 | c0005 | t0012 | g0249 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG02559 | hp2 | a0002 | c0002 | t0005 | g0081 | AFR | ACB | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03471 | hp1 | a0002 | c0002 | t0005 | g0006 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG03471 | hp2 | a0002 | c0008 | t0008 | g0191 | AFR | MSL | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG06807 | hp1 | a0004 | c0005 | t0013 | g0236 | AFR | USA | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| HG06807 | hp2 | a0007 | c0019 | t0017 | g0314 | AFR | USA | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20300 | hp1 | a0006 | c0007 | t0060 | g0032 | AFR | USA | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA20300 | hp2 | a0004 | c0005 | t0013 | g0298 | AFR | USA | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA21309 | hp1 | a0001 | c0006 | t0001 | g0099 | AFR | LWK | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| NA21309 | hp2 | a0002 | c0002 | t0005 | g0028 | AFR | LWK | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0075 | REF | REF | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0138 | REF | REF | PPARGC1B_chr5_149725310_149860022 | PPARGC1B | chr5 | 149725310 | 149860022 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149820445 | G | A | 1 | a0010 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.91G>A | p.Gly31Arg | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/12 | 124/10569 | 91/3072 | 31/1023 | chr5 | 149820445 | |||
| chr5:149826839 | C | T | 1 | a0017 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.419C>T | p.Pro140Leu | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/12 | 452/10569 | 419/3072 | 140/1023 | chr5 | 149826839 | |||
| chr5:149826860 | C | A | 1 | a0014 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.440C>A | p.Ala147Asp | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/12 | 473/10569 | 440/3072 | 147/1023 | chr5 | 149826860 | |||
| chr5:149832680 | G | C | 6 | a0004 a0005 a0008 others(3): Show |
40 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(37): Show |
missense_variant | MODERATE | c.607G>C | p.Ala203Pro | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 640/10569 | 607/3072 | 203/1023 | chr5 | 149832680 | |||
| chr5:149832863 | C | A | 1 | a0014 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.790C>A | p.Pro264Thr | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 823/10569 | 790/3072 | 264/1023 | chr5 | 149832863 | |||
| chr5:149832867 | G | A | 2 | a0003 a0011 |
31 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(28): Show |
missense_variant | MODERATE | c.794G>A | p.Arg265Gln | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 827/10569 | 794/3072 | 265/1023 | chr5 | 149832867 | |||
| chr5:149832908 | G | A | 2 | a0004 a0017 |
25 | HG00639.hp2 HG01106.hp2 HG01109.hp1 others(22): Show |
missense_variant | MODERATE | c.835G>A | p.Val279Ile | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 868/10569 | 835/3072 | 279/1023 | chr5 | 149832908 | |||
| chr5:149832947 | C | A | 3 | a0002 a0009 a0015 |
44 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(41): Show |
missense_variant | MODERATE | c.874C>A | p.Arg292Ser | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 907/10569 | 874/3072 | 292/1023 | chr5 | 149832947 | |||
| chr5:149833061 | C | T | 1 | a0006 | 7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.988C>T | p.Arg330Trp | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1021/10569 | 988/3072 | 330/1023 | chr5 | 149833061 | |||
| chr5:149833124 | G | A | 2 | a0009 a0015 |
3 | HG02451.hp2 HG03195.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1051G>A | p.Val351Met | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1084/10569 | 1051/3072 | 351/1023 | chr5 | 149833124 | |||
| chr5:149833161 | C | T | 1 | a0008 | 3 | HG02647.hp1 HG02818.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.1088C>T | p.Thr363Met | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1121/10569 | 1088/3072 | 363/1023 | chr5 | 149833161 | |||
| chr5:149833239 | C | A | 1 | a0006 | 7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.1166C>A | p.Ser389Tyr | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1199/10569 | 1166/3072 | 389/1023 | chr5 | 149833239 | |||
| chr5:149833404 | A | G | 1 | a0011 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1331A>G | p.Glu444Gly | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1364/10569 | 1331/3072 | 444/1023 | chr5 | 149833404 | |||
| chr5:149833572 | C | T | 2 | a0008 a0013 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.1499C>T | p.Ser500Leu | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1532/10569 | 1499/3072 | 500/1023 | chr5 | 149833572 | |||
| chr5:149836596 | C | T | 1 | a0007 | 3 | HG02257.hp2 HG03225.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.2141C>T | p.Pro714Leu | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/12 | 2174/10569 | 2141/3072 | 714/1023 | chr5 | 149836596 | |||
| chr5:149840090 | G | A | 1 | a0012 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.2668G>A | p.Ala890Thr | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/12 | 2701/10569 | 2668/3072 | 890/1023 | chr5 | 149840090 | |||
| chr5:149842279 | T | G | 1 | a0009 | 2 | HG02451.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.2718T>G | p.Ile906Met | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/12 | 2751/10569 | 2718/3072 | 906/1023 | chr5 | 149842279 | |||
| chr5:149842295 | G | T | 1 | a0016 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.2734G>T | p.Asp912Tyr | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/12 | 2767/10569 | 2734/3072 | 912/1023 | chr5 | 149842295 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149820480 | T | C | 10 | a0001c0004 a0001c0006 a0001c0009 others(7): Show |
57 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(54): Show |
synonymous_variant | LOW | c.126T>C | p.Leu42Leu | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/12 | 159/10569 | 126/3072 | 42/1023 | chr5 | 149820480 | |||
| chr5:149820516 | G | A | 1 | a0001c0024 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.162G>A | p.Ser54Ser | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/12 | 195/10569 | 162/3072 | 54/1023 | chr5 | 149820516 | |||
| chr5:149833051 | G | T | 1 | a0001c0018 | 3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
synonymous_variant | LOW | c.978G>T | p.Arg326Arg | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1011/10569 | 978/3072 | 326/1023 | chr5 | 149833051 | |||
| chr5:149833237 | G | A | 8 | a0001c0004 a0001c0017 a0001c0022 others(5): Show |
37 | HG00280.hp2 HG00735.hp2 HG01069.hp1 others(34): Show |
synonymous_variant | LOW | c.1164G>A | p.Pro388Pro | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1197/10569 | 1164/3072 | 388/1023 | chr5 | 149833237 | |||
| chr5:149833243 | G | A | 1 | a0001c0022 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1170G>A | p.Ser390Ser | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1203/10569 | 1170/3072 | 390/1023 | chr5 | 149833243 | |||
| chr5:149833654 | C | T | 1 | a0002c0014 | 4 | HG00609.hp2 HG02165.hp1 HG03942.hp2 others(1): Show |
synonymous_variant | LOW | c.1581C>T | p.Asp527Asp | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1614/10569 | 1581/3072 | 527/1023 | chr5 | 149833654 | |||
| chr5:149833762 | G | A | 1 | a0001c0030 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1689G>A | p.Pro563Pro | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/12 | 1722/10569 | 1689/3072 | 563/1023 | chr5 | 149833762 | |||
| chr5:149835343 | A | G | 1 | a0006c0007 | 7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
synonymous_variant | LOW | c.1785A>G | p.Thr595Thr | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/12 | 1818/10569 | 1785/3072 | 595/1023 | chr5 | 149835343 | |||
| chr5:149836432 | A | C | 1 | a0007c0023 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1977A>C | p.Pro659Pro | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/12 | 2010/10569 | 1977/3072 | 659/1023 | chr5 | 149836432 | |||
| chr5:149836579 | G | A | 2 | a0001c0006 a0001c0010 |
13 | HG01496.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
synonymous_variant | LOW | c.2124G>A | p.Val708Val | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/12 | 2157/10569 | 2124/3072 | 708/1023 | chr5 | 149836579 | |||
| chr5:149836693 | C | T | 4 | a0003c0003 a0003c0012 a0005c0026 others(1): Show |
32 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(29): Show |
synonymous_variant | LOW | c.2238C>T | p.Gly746Gly | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/12 | 2271/10569 | 2238/3072 | 746/1023 | chr5 | 149836693 | |||
| chr5:149836741 | C | T | 3 | a0003c0003 a0003c0012 a0011c0028 |
31 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(28): Show |
synonymous_variant | LOW | c.2286C>T | p.Ala762Ala | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/12 | 2319/10569 | 2286/3072 | 762/1023 | chr5 | 149836741 | |||
| chr5:149840089 | C | T | 1 | a0001c0033 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.2667C>T | p.His889His | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/12 | 2700/10569 | 2667/3072 | 889/1023 | chr5 | 149840089 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149847704 | T | TA | 6 | a0003c0003t0004 a0003c0003t0011 a0003c0003t0033 others(3): Show |
30 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*160dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 161 | INFO_REALIGN_3_PRIME | chr5 | 149847704 | |||||
| chr5:149847773 | C | T | 1 | a0002c0008t0071 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*215C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 215 | chr5 | 149847773 | ||||||
| chr5:149847881 | C | T | 1 | a0001c0001t0070 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*323C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 323 | chr5 | 149847881 | ||||||
| chr5:149847977 | T | C | 5 | a0003c0003t0004 a0003c0003t0011 a0003c0003t0033 others(2): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*419T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 419 | chr5 | 149847977 | ||||||
| chr5:149847997 | T | C | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*439T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 439 | chr5 | 149847997 | ||||||
| chr5:149848003 | C | T | 1 | a0016c0032t0069 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*445C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 445 | chr5 | 149848003 | ||||||
| chr5:149848125 | A | G | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*567A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 567 | chr5 | 149848125 | ||||||
| chr5:149848175 | G | A | 1 | a0001c0010t0038 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*617G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 617 | chr5 | 149848175 | ||||||
| chr5:149848298 | A | T | 17 | a0001c0009t0064 a0002c0002t0005 a0002c0002t0008 others(14): Show |
45 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*740A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 740 | chr5 | 149848298 | ||||||
| chr5:149848301 | T | C | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*743T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 743 | chr5 | 149848301 | ||||||
| chr5:149848312 | T | C | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*754T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 754 | chr5 | 149848312 | ||||||
| chr5:149848366 | G | T | 1 | a0001c0001t0019 | 4 | HG00099.hp1 HG01109.hp2 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*808G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 808 | chr5 | 149848366 | ||||||
| chr5:149848500 | C | T | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*942C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 942 | chr5 | 149848500 | ||||||
| chr5:149848711 | A | G | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1153A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1153 | chr5 | 149848711 | ||||||
| chr5:149848792 | G | A | 1 | a0001c0001t0039 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1234G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1234 | chr5 | 149848792 | ||||||
| chr5:149848799 | T | C | 1 | a0001c0001t0040 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1241T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1241 | chr5 | 149848799 | ||||||
| chr5:149848958 | T | G | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1400T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1400 | chr5 | 149848958 | ||||||
| chr5:149849073 | A | G | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1515A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1515 | chr5 | 149849073 | ||||||
| chr5:149849085 | C | T | 45 | a0001c0004t0006 a0001c0004t0018 a0001c0004t0024 others(42): Show |
121 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1527C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1527 | chr5 | 149849085 | ||||||
| chr5:149849095 | T | C | 2 | a0001c0018t0029 a0001c0018t0058 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1537T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1537 | chr5 | 149849095 | ||||||
| chr5:149849099 | AT | A | 6 | a0006c0007t0016 a0006c0007t0059 a0006c0007t0060 others(3): Show |
11 | HG02451.hp1 HG02647.hp1 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1551delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1551 | INFO_REALIGN_3_PRIME | chr5 | 149849099 | |||||
| chr5:149849170 | T | A | 1 | a0002c0008t0063 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1612T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1612 | chr5 | 149849170 | ||||||
| chr5:149849317 | T | A | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1759T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1759 | chr5 | 149849317 | ||||||
| chr5:149849385 | T | C | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1827T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1827 | chr5 | 149849385 | ||||||
| chr5:149849408 | G | A | 3 | a0001c0017t0017 a0007c0019t0017 a0007c0023t0017 |
4 | HG02257.hp2 HG02572.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1850G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1850 | chr5 | 149849408 | ||||||
| chr5:149849430 | C | T | 1 | a0001c0001t0057 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1872C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1872 | chr5 | 149849430 | ||||||
| chr5:149849487 | C | A | 3 | a0006c0007t0016 a0006c0007t0059 a0006c0007t0060 |
7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1929C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1929 | chr5 | 149849487 | ||||||
| chr5:149849496 | C | T | 1 | a0005c0026t0034 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1938C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1938 | chr5 | 149849496 | ||||||
| chr5:149849522 | C | T | 16 | a0002c0002t0005 a0002c0002t0008 a0002c0002t0010 others(13): Show |
44 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1964C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 1964 | chr5 | 149849522 | ||||||
| chr5:149849705 | G | C | 3 | a0001c0018t0029 a0001c0018t0058 a0010c0021t0061 |
4 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2147G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2147 | chr5 | 149849705 | ||||||
| chr5:149849783 | G | A | 1 | a0001c0001t0041 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2225G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2225 | chr5 | 149849783 | ||||||
| chr5:149849797 | G | C | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2239G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2239 | chr5 | 149849797 | ||||||
| chr5:149849809 | G | A | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2251G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2251 | chr5 | 149849809 | ||||||
| chr5:149850021 | A | G | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2463A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2463 | chr5 | 149850021 | ||||||
| chr5:149850039 | A | G | 1 | a0006c0007t0060 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2481A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2481 | chr5 | 149850039 | ||||||
| chr5:149850155 | A | T | 1 | a0001c0001t0028 | 2 | HG00741.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2597A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2597 | chr5 | 149850155 | ||||||
| chr5:149850259 | G | T | 12 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(9): Show |
38 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2701G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2701 | chr5 | 149850259 | ||||||
| chr5:149850390 | G | C | 1 | a0001c0006t0042 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2832G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2832 | chr5 | 149850390 | ||||||
| chr5:149850512 | G | A | 1 | a0002c0002t0065 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2954G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2954 | chr5 | 149850512 | ||||||
| chr5:149850548 | C | T | 4 | a0002c0002t0025 a0006c0007t0016 a0006c0007t0059 others(1): Show |
10 | HG00738.hp1 HG01993.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2990C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 2990 | chr5 | 149850548 | ||||||
| chr5:149850779 | C | T | 2 | a0001c0010t0038 a0001c0010t0056 |
2 | HG02630.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3221C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3221 | chr5 | 149850779 | ||||||
| chr5:149850780 | G | A | 1 | a0001c0001t0043 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3222G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3222 | chr5 | 149850780 | ||||||
| chr5:149850955 | C | T | 1 | a0004c0005t0055 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3397C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3397 | chr5 | 149850955 | ||||||
| chr5:149851093 | G | A | 1 | a0001c0009t0064 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3535G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3535 | chr5 | 149851093 | ||||||
| chr5:149851167 | T | C | 83 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(80): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*3609T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3609 | chr5 | 149851167 | ||||||
| chr5:149851169 | G | A | 8 | a0001c0004t0006 a0001c0004t0030 a0001c0004t0062 others(5): Show |
21 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3611G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3611 | chr5 | 149851169 | ||||||
| chr5:149851182 | T | C | 13 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(10): Show |
39 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3624T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3624 | chr5 | 149851182 | ||||||
| chr5:149851224 | C | T | 13 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(10): Show |
39 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3666C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3666 | chr5 | 149851224 | ||||||
| chr5:149851267 | G | C | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3709G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3709 | chr5 | 149851267 | ||||||
| chr5:149851269 | T | TACTGG | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3711_*3712insACTG others(1): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3712 | chr5 | 149851269 | ||||||
| chr5:149851288 | A | G | 3 | a0008c0016t0026 a0008c0016t0036 a0013c0027t0037 |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3730A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3730 | chr5 | 149851288 | ||||||
| chr5:149851389 | A | G | 10 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(7): Show |
35 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3831A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3831 | chr5 | 149851389 | ||||||
| chr5:149851544 | T | C | 1 | a0001c0001t0044 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3986T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 3986 | chr5 | 149851544 | ||||||
| chr5:149851589 | G | A | 5 | a0001c0001t0045 a0001c0001t0047 a0001c0009t0027 others(2): Show |
5 | HG01243.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4031G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4031 | chr5 | 149851589 | ||||||
| chr5:149851600 | C | A | 1 | a0010c0021t0061 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4042C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4042 | chr5 | 149851600 | ||||||
| chr5:149851627 | T | TC | 10 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(7): Show |
35 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4071dupC | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4072 | INFO_REALIGN_3_PRIME | chr5 | 149851627 | |||||
| chr5:149851655 | GT | G | 2 | a0003c0003t0011 a0011c0028t0011 |
7 | HG01928.hp2 HG01952.hp1 HG01978.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4098delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4098 | chr5 | 149851655 | ||||||
| chr5:149851769 | G | T | 46 | a0001c0004t0006 a0001c0004t0018 a0001c0004t0024 others(43): Show |
122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*4211G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4211 | chr5 | 149851769 | ||||||
| chr5:149851816 | A | G | 3 | a0001c0018t0029 a0001c0018t0058 a0010c0021t0061 |
4 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4258A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4258 | chr5 | 149851816 | ||||||
| chr5:149851956 | C | T | 23 | a0001c0004t0006 a0001c0004t0018 a0001c0004t0024 others(20): Show |
70 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*4398C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4398 | chr5 | 149851956 | ||||||
| chr5:149851958 | A | C | 3 | a0001c0018t0029 a0001c0018t0058 a0010c0021t0061 |
4 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4400A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4400 | chr5 | 149851958 | ||||||
| chr5:149851982 | A | C | 3 | a0001c0018t0029 a0001c0018t0058 a0010c0021t0061 |
4 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4424A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4424 | chr5 | 149851982 | ||||||
| chr5:149852091 | A | G | 3 | a0001c0018t0029 a0001c0018t0058 a0010c0021t0061 |
4 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4533A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4533 | chr5 | 149852091 | ||||||
| chr5:149852092 | C | A | 9 | a0002c0002t0005 a0002c0002t0010 a0002c0002t0025 others(6): Show |
32 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*4534C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4534 | chr5 | 149852092 | ||||||
| chr5:149852139 | G | A | 1 | a0001c0001t0053 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4581G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4581 | chr5 | 149852139 | ||||||
| chr5:149852163 | A | G | 1 | a0005c0026t0034 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4605A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4605 | chr5 | 149852163 | ||||||
| chr5:149852223 | G | A | 10 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(7): Show |
35 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4665G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4665 | chr5 | 149852223 | ||||||
| chr5:149852267 | A | G | 41 | a0001c0004t0006 a0001c0004t0018 a0001c0004t0024 others(38): Show |
116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*4709A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4709 | chr5 | 149852267 | ||||||
| chr5:149852271 | G | A | 1 | a0002c0002t0066 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4713G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4713 | chr5 | 149852271 | ||||||
| chr5:149852299 | C | A | 1 | a0001c0001t0045 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4741C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4741 | chr5 | 149852299 | ||||||
| chr5:149852388 | C | T | 1 | a0010c0021t0061 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4830C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 4830 | chr5 | 149852388 | ||||||
| chr5:149852650 | C | T | 10 | a0001c0004t0006 a0001c0004t0018 a0001c0004t0024 others(7): Show |
28 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5092C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5092 | chr5 | 149852650 | ||||||
| chr5:149852708 | C | CT | 20 | a0001c0001t0009 a0001c0009t0009 a0001c0010t0009 others(17): Show |
61 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*5167dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5168 | INFO_REALIGN_3_PRIME | chr5 | 149852708 | |||||
| chr5:149852708 | C | CTTT | 5 | a0001c0004t0006 a0001c0004t0018 a0001c0004t0062 others(2): Show |
19 | HG01168.hp1 HG02280.hp1 HG02293.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5165_*5167dupTTT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5168 | INFO_REALIGN_3_PRIME | chr5 | 149852708 | |||||
| chr5:149852708 | CT | C | 9 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0023 others(6): Show |
17 | HG00558.hp1 HG02040.hp2 HG02165.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5167delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5167 | INFO_REALIGN_3_PRIME | chr5 | 149852708 | |||||
| chr5:149852744 | A | C | 89 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(86): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*5186A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5186 | chr5 | 149852744 | ||||||
| chr5:149852745 | G | A | 9 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(6): Show |
34 | HG00140.hp2 HG00280.hp1 HG01074.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*5187G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5187 | chr5 | 149852745 | ||||||
| chr5:149852962 | A | G | 11 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(8): Show |
36 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5404A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5404 | chr5 | 149852962 | ||||||
| chr5:149853261 | G | A | 1 | a0001c0001t0047 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5703G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5703 | chr5 | 149853261 | ||||||
| chr5:149853545 | T | C | 1 | a0001c0001t0051 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5987T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5987 | chr5 | 149853545 | ||||||
| chr5:149853547 | C | A | 12 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(9): Show |
41 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*5989C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 5989 | chr5 | 149853547 | ||||||
| chr5:149853574 | G | A | 2 | a0001c0001t0021 a0001c0001t0070 |
4 | HG00741.hp1 HG01258.hp1 HG01891.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6016G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 6016 | chr5 | 149853574 | ||||||
| chr5:149853623 | C | T | 8 | a0001c0018t0029 a0001c0018t0058 a0003c0003t0004 others(5): Show |
33 | HG00140.hp2 HG00280.hp1 HG01074.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*6065C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 6065 | chr5 | 149853623 | ||||||
| chr5:149853867 | A | T | 1 | a0001c0001t0051 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6309A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 6309 | chr5 | 149853867 | ||||||
| chr5:149853917 | C | G | 2 | a0004c0005t0022 a0004c0005t0049 |
4 | HG02165.hp2 NA18949.hp2 NA18990.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6359C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 6359 | chr5 | 149853917 | ||||||
| chr5:149853992 | A | G | 3 | a0001c0001t0003 a0001c0001t0020 a0001c0001t0051 |
27 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6434A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 6434 | chr5 | 149853992 | ||||||
| chr5:149854330 | G | T | 1 | a0001c0001t0054 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6772G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 6772 | chr5 | 149854330 | ||||||
| chr5:149854387 | T | TTG | 7 | a0003c0003t0004 a0003c0003t0011 a0003c0003t0033 others(4): Show |
31 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*6848_*6849dupTG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 6850 | INFO_REALIGN_3_PRIME | chr5 | 149854387 | |||||
| chr5:149854461 | G | A | 1 | a0001c0001t0007 | 9 | NA18944.hp2 NA18979.hp2 NA18980.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6903G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 6903 | chr5 | 149854461 | ||||||
| chr5:149854672 | C | A | 51 | a0001c0001t0012 a0001c0001t0040 a0001c0001t0048 others(48): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*7114C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 7114 | chr5 | 149854672 | ||||||
| chr5:149854673 | A | T | 51 | a0001c0001t0012 a0001c0001t0040 a0001c0001t0048 others(48): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*7115A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 7115 | chr5 | 149854673 | ||||||
| chr5:149854682 | T | C | 2 | a0001c0018t0029 a0001c0018t0058 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7124T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 7124 | chr5 | 149854682 | ||||||
| chr5:149854938 | C | T | 13 | a0002c0002t0005 a0002c0002t0010 a0002c0002t0025 others(10): Show |
42 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*7380C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 12/12 | 7380 | chr5 | 149854938 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149730441 | G | A | 2 | a0001c0001t0001g0002 a0001c0006t0042g0001 |
2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.78+21G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149730441 | |||||||
| chr5:149730552 | C | G | 3 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 |
3 | HG02451.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.78+132C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149730552 | |||||||
| chr5:149731018 | G | A | 4 | a0002c0002t0005g0006 a0002c0002t0008g0003 a0009c0020t0008g0004 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+598G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731018 | |||||||
| chr5:149731066 | G | A | 37 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0003g0020 others(34): Show |
37 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.78+646G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731066 | |||||||
| chr5:149731242 | G | T | 7 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0002c0008t0008g0319 others(4): Show |
7 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+822G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731242 | |||||||
| chr5:149731331 | C | G | 1 | a0001c0006t0001g0313 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.78+911C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731331 | |||||||
| chr5:149731403 | A | C | 50 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0285 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.78+983A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731403 | |||||||
| chr5:149731420 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(76): Show |
79 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.78+1000C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731420 | |||||||
| chr5:149731437 | T | C | 8 | a0001c0001t0001g0010 a0001c0017t0017g0014 a0004c0005t0001g0011 others(5): Show |
8 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+1017T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731437 | |||||||
| chr5:149731620 | T | C | 7 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0002c0008t0008g0319 others(4): Show |
7 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+1200T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731620 | |||||||
| chr5:149731661 | T | C | 1 | a0001c0001t0003g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.78+1241T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731661 | |||||||
| chr5:149731711 | G | T | 1 | a0001c0001t0002g0269 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.78+1291G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731711 | |||||||
| chr5:149731972 | C | T | 49 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0285 others(46): Show |
49 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.78+1552C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149731972 | |||||||
| chr5:149732045 | G | GGT | 5 | a0001c0001t0001g0190 a0001c0001t0001g0312 a0001c0001t0015g0189 others(2): Show |
5 | HG00558.hp1 HG03471.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+1657_78+1658dup others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149732045 | ||||||
| chr5:149732045 | GGT | G | 17 | a0001c0001t0002g0134 a0001c0001t0020g0126 a0001c0006t0001g0313 others(14): Show |
17 | HG02451.hp1 HG02723.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.78+1657_78+1658del others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149732045 | ||||||
| chr5:149732045 | GGTGT | G | 76 | a0001c0001t0001g0053 a0001c0001t0001g0061 a0001c0001t0001g0062 others(73): Show |
76 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.78+1655_78+1658del others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149732045 | ||||||
| chr5:149732045 | GGTGTGT | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0047 others(105): Show |
108 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.78+1653_78+1658del others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149732045 | ||||||
| chr5:149732045 | GGTGTGTG others(1): Show |
G | 54 | a0001c0001t0001g0018 a0001c0001t0001g0271 a0001c0001t0001g0280 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.78+1651_78+1658del others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149732045 | ||||||
| chr5:149732197 | C | A | 1 | a0002c0008t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.78+1777C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732197 | |||||||
| chr5:149732214 | C | A | 126 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.78+1794C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732214 | |||||||
| chr5:149732374 | T | C | 8 | a0001c0001t0001g0010 a0001c0017t0017g0014 a0004c0005t0001g0011 others(5): Show |
8 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+1954T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732374 | |||||||
| chr5:149732430 | G | T | 1 | a0003c0012t0014g0120 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.78+2010G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732430 | |||||||
| chr5:149732586 | T | C | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+2166T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732586 | |||||||
| chr5:149732603 | A | G | 176 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.78+2183A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732603 | |||||||
| chr5:149732632 | T | A | 52 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(49): Show |
52 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.78+2212T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732632 | |||||||
| chr5:149732694 | C | G | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+2274C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732694 | |||||||
| chr5:149732695 | G | A | 7 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0002c0008t0008g0319 others(4): Show |
7 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+2275G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732695 | |||||||
| chr5:149732737 | T | G | 50 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0285 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.78+2317T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732737 | |||||||
| chr5:149732909 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.78+2489C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732909 | |||||||
| chr5:149732968 | C | T | 1 | a0001c0009t0046g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.78+2548C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149732968 | |||||||
| chr5:149733053 | C | T | 2 | a0005c0011t0009g0133 a0005c0011t0027g0132 |
2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.78+2633C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149733053 | |||||||
| chr5:149733096 | G | C | 1 | a0001c0004t0006g0193 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.78+2676G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149733096 | |||||||
| chr5:149733295 | A | C | 1 | a0001c0001t0007g0188 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.78+2875A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149733295 | |||||||
| chr5:149733390 | T | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.78+2970T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149733390 | |||||||
| chr5:149733478 | G | T | 315 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(312): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.78+3058G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149733478 | |||||||
| chr5:149733533 | G | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.78+3113G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149733533 | |||||||
| chr5:149733561 | G | A | 3 | a0001c0001t0002g0274 a0001c0001t0002g0275 a0001c0001t0002g0276 |
3 | HG01071.hp2 HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.78+3141G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149733561 | |||||||
| chr5:149733570 | C | A | 7 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0002c0008t0008g0319 others(4): Show |
7 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+3150C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149733570 | |||||||
| chr5:149734011 | G | C | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.78+3591G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734011 | |||||||
| chr5:149734027 | TA | T | 4 | a0001c0001t0001g0092 a0001c0001t0002g0093 a0001c0001t0012g0090 others(1): Show |
4 | HG00544.hp1 HG02083.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+3613delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149734027 | ||||||
| chr5:149734050 | G | A | 1 | a0004c0005t0001g0139 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.78+3630G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734050 | |||||||
| chr5:149734151 | G | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(76): Show |
79 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.78+3731G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734151 | |||||||
| chr5:149734235 | T | TCGCTTGA others(27): Show |
8 | a0001c0001t0001g0010 a0001c0017t0017g0014 a0004c0005t0001g0011 others(5): Show |
8 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+3818_78+3851dup others(34): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149734235 | ||||||
| chr5:149734247 | G | A | 2 | a0001c0001t0001g0002 a0001c0006t0042g0001 |
2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.78+3827G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734247 | |||||||
| chr5:149734321 | C | CA | 28 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0002g0050 others(25): Show |
28 | HG00438.hp1 HG00741.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.78+3925dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149734321 | ||||||
| chr5:149734321 | CA | C | 122 | a0001c0001t0001g0186 a0001c0001t0001g0201 a0001c0001t0001g0206 others(119): Show |
122 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.78+3925delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149734321 | ||||||
| chr5:149734321 | CAA | C | 10 | a0001c0001t0002g0308 a0001c0001t0047g0265 a0002c0002t0005g0266 others(7): Show |
10 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+3924_78+3925del others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149734321 | ||||||
| chr5:149734446 | C | G | 2 | a0001c0010t0038g0185 a0002c0008t0071g0184 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.78+4026C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734446 | |||||||
| chr5:149734585 | G | A | 53 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(50): Show |
53 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.78+4165G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734585 | |||||||
| chr5:149734593 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.78+4173G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734593 | |||||||
| chr5:149734613 | C | T | 2 | a0004c0005t0001g0121 a0008c0016t0036g0122 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78+4193C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734613 | |||||||
| chr5:149734623 | T | G | 1 | a0015c0029t0008g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+4203T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734623 | |||||||
| chr5:149734630 | A | T | 1 | a0001c0001t0002g0307 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.78+4210A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734630 | |||||||
| chr5:149734661 | T | C | 176 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.78+4241T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734661 | |||||||
| chr5:149734789 | G | A | 50 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0285 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.78+4369G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734789 | |||||||
| chr5:149734876 | T | C | 50 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0285 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.78+4456T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149734876 | |||||||
| chr5:149735087 | T | C | 39 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0285 others(36): Show |
39 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.78+4667T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735087 | |||||||
| chr5:149735180 | T | C | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.78+4760T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735180 | |||||||
| chr5:149735368 | G | A | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.78+4948G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735368 | |||||||
| chr5:149735402 | T | C | 1 | a0015c0029t0008g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+4982T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735402 | |||||||
| chr5:149735507 | C | G | 1 | a0015c0029t0008g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+5087C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735507 | |||||||
| chr5:149735523 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+5103G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735523 | |||||||
| chr5:149735530 | G | C | 1 | a0001c0001t0019g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.78+5110G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735530 | |||||||
| chr5:149735588 | A | C | 36 | a0001c0001t0001g0280 a0001c0001t0001g0285 a0001c0001t0002g0274 others(33): Show |
36 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.78+5168A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735588 | |||||||
| chr5:149735592 | T | C | 40 | a0001c0001t0001g0149 a0001c0001t0001g0201 a0001c0001t0001g0206 others(37): Show |
40 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.78+5172T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735592 | |||||||
| chr5:149735759 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+5339G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735759 | |||||||
| chr5:149735907 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01361.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.78+5487C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149735907 | |||||||
| chr5:149736001 | G | A | 1 | a0001c0001t0003g0151 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.78+5581G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736001 | |||||||
| chr5:149736031 | A | G | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.78+5611A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736031 | |||||||
| chr5:149736074 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.78+5654G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736074 | |||||||
| chr5:149736099 | A | G | 50 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0285 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.78+5679A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736099 | |||||||
| chr5:149736114 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+5694C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736114 | |||||||
| chr5:149736185 | T | G | 1 | a0007c0019t0017g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.78+5765T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736185 | |||||||
| chr5:149736367 | C | CT | 9 | a0001c0006t0001g0313 a0001c0009t0009g0130 a0002c0008t0005g0129 others(6): Show |
9 | HG02132.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.78+5960dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149736367 | ||||||
| chr5:149736367 | CT | C | 11 | a0001c0006t0001g0099 a0001c0006t0001g0100 a0001c0006t0001g0316 others(8): Show |
11 | HG02451.hp1 HG02451.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.78+5960delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149736367 | ||||||
| chr5:149736601 | A | G | 1 | a0001c0004t0006g0193 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.78+6181A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736601 | |||||||
| chr5:149736609 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.78+6189A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736609 | |||||||
| chr5:149736749 | A | T | 39 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0285 others(36): Show |
39 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.78+6329A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736749 | |||||||
| chr5:149736917 | T | G | 2 | a0004c0005t0001g0121 a0008c0016t0036g0122 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78+6497T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736917 | |||||||
| chr5:149736941 | C | T | 1 | a0003c0003t0004g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.78+6521C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149736941 | |||||||
| chr5:149737117 | C | T | 1 | a0001c0001t0023g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.78+6697C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737117 | |||||||
| chr5:149737143 | A | G | 2 | a0001c0001t0001g0312 a0015c0029t0008g0270 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.78+6723A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737143 | |||||||
| chr5:149737345 | G | T | 2 | a0005c0026t0034g0310 a0010c0021t0061g0311 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.78+6925G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737345 | |||||||
| chr5:149737441 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(256): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.78+7021T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737441 | |||||||
| chr5:149737470 | C | T | 2 | a0005c0026t0034g0310 a0010c0021t0061g0311 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.78+7050C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737470 | |||||||
| chr5:149737629 | G | A | 1 | a0001c0001t0047g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.78+7209G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737629 | |||||||
| chr5:149737659 | G | A | 4 | a0002c0002t0005g0006 a0002c0002t0008g0003 a0009c0020t0008g0004 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+7239G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737659 | |||||||
| chr5:149737747 | G | A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+7327G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737747 | |||||||
| chr5:149737845 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.78+7425T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149737845 | |||||||
| chr5:149738014 | G | T | 2 | a0001c0001t0001g0002 a0001c0006t0042g0001 |
2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.78+7594G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738014 | |||||||
| chr5:149738082 | C | T | 1 | a0008c0016t0036g0122 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.78+7662C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738082 | |||||||
| chr5:149738093 | A | G | 7 | a0001c0006t0001g0313 a0001c0009t0009g0130 a0002c0008t0005g0129 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+7673A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738093 | |||||||
| chr5:149738132 | CATCACTC others(128): Show |
C | 1 | a0004c0005t0055g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.78+7747_78+7881del | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149738132 | ||||||
| chr5:149738264 | G | A | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.78+7844G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738264 | |||||||
| chr5:149738323 | C | G | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.78+7903C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738323 | |||||||
| chr5:149738539 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+8119A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738539 | |||||||
| chr5:149738607 | A | AT | 43 | a0001c0001t0001g0149 a0001c0001t0001g0201 a0001c0001t0001g0206 others(40): Show |
43 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.78+8200dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149738607 | ||||||
| chr5:149738696 | A | G | 1 | a0015c0029t0008g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+8276A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738696 | |||||||
| chr5:149738789 | G | A | 2 | a0001c0001t0001g0312 a0015c0029t0008g0270 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.78+8369G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738789 | |||||||
| chr5:149738837 | C | T | 2 | a0002c0014t0005g0259 a0002c0014t0005g0260 |
2 | HG02165.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.78+8417C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738837 | |||||||
| chr5:149738849 | C | A | 1 | a0001c0001t0002g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.78+8429C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149738849 | |||||||
| chr5:149739126 | A | G | 20 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0002g0148 others(17): Show |
20 | HG00408.hp2 HG02040.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.78+8706A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149739126 | |||||||
| chr5:149739131 | A | C | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+8711A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149739131 | |||||||
| chr5:149739278 | G | A | 257 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.78+8858G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149739278 | |||||||
| chr5:149739423 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.78+9003G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149739423 | |||||||
| chr5:149739620 | G | A | 1 | a0001c0009t0046g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.78+9200G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149739620 | |||||||
| chr5:149739857 | A | G | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.78+9437A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149739857 | |||||||
| chr5:149739887 | A | G | 7 | a0001c0006t0001g0313 a0001c0009t0009g0130 a0002c0008t0005g0129 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+9467A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149739887 | |||||||
| chr5:149739897 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+9477G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149739897 | |||||||
| chr5:149740115 | T | C | 4 | a0001c0004t0018g0031 a0006c0007t0016g0040 a0006c0007t0059g0033 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+9695T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740115 | |||||||
| chr5:149740240 | T | G | 49 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0001g0312 others(46): Show |
49 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.78+9820T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740240 | |||||||
| chr5:149740252 | T | C | 36 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0003g0020 others(33): Show |
36 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.78+9832T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740252 | |||||||
| chr5:149740255 | A | G | 1 | a0001c0009t0002g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.78+9835A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740255 | |||||||
| chr5:149740272 | G | A | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78+9852G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740272 | |||||||
| chr5:149740320 | A | G | 1 | a0001c0009t0046g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.78+9900A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740320 | |||||||
| chr5:149740378 | G | A | 4 | a0001c0010t0001g0056 a0002c0002t0008g0055 a0005c0011t0009g0054 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+9958G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740378 | |||||||
| chr5:149740416 | T | G | 177 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.78+9996T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740416 | |||||||
| chr5:149740424 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+10004C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740424 | |||||||
| chr5:149740446 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+10026G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740446 | |||||||
| chr5:149740823 | G | C | 2 | a0002c0008t0005g0129 a0005c0011t0001g0128 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.78+10403G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740823 | |||||||
| chr5:149740900 | G | C | 3 | a0001c0001t0001g0233 a0001c0001t0015g0232 a0004c0005t0022g0234 |
3 | NA18948.hp1 NA18949.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.78+10480G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740900 | |||||||
| chr5:149740930 | C | T | 1 | a0003c0003t0004g0305 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.78+10510C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740930 | |||||||
| chr5:149740934 | C | T | 1 | a0001c0001t0007g0188 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.78+10514C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149740934 | |||||||
| chr5:149741116 | C | A | 1 | a0002c0002t0010g0264 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.78+10696C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741116 | |||||||
| chr5:149741322 | G | A | 10 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0001g0244 others(7): Show |
10 | HG00558.hp2 HG01106.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+10902G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741322 | |||||||
| chr5:149741351 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+10931A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741351 | |||||||
| chr5:149741410 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.78+10990G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741410 | |||||||
| chr5:149741534 | C | A | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78+11114C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741534 | |||||||
| chr5:149741626 | C | CT | 33 | a0001c0001t0001g0271 a0001c0001t0003g0103 a0001c0001t0007g0106 others(30): Show |
33 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.78+11222dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149741626 | ||||||
| chr5:149741626 | CT | C | 103 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.78+11222delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149741626 | ||||||
| chr5:149741652 | G | C | 1 | a0015c0029t0008g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+11232G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741652 | |||||||
| chr5:149741753 | G | A | 2 | a0001c0001t0001g0312 a0015c0029t0008g0270 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.78+11333G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741753 | |||||||
| chr5:149741786 | C | T | 1 | a0016c0032t0069g0127 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.78+11366C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741786 | |||||||
| chr5:149741841 | G | A | 7 | a0001c0006t0001g0316 a0001c0009t0064g0261 a0001c0030t0031g0320 others(4): Show |
7 | HG02451.hp1 HG03041.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+11421G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741841 | |||||||
| chr5:149741907 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+11487A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741907 | |||||||
| chr5:149741909 | C | G | 1 | a0001c0001t0002g0093 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.78+11489C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741909 | |||||||
| chr5:149741922 | G | A | 2 | a0005c0026t0034g0310 a0010c0021t0061g0311 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.78+11502G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741922 | |||||||
| chr5:149741930 | T | C | 1 | a0015c0029t0008g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+11510T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149741930 | |||||||
| chr5:149742008 | G | A | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78+11588G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149742008 | |||||||
| chr5:149742062 | A | G | 1 | a0004c0015t0001g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78+11642A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149742062 | |||||||
| chr5:149742204 | T | C | 177 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.78+11784T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149742204 | |||||||
| chr5:149742271 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0015g0189 |
2 | HG00558.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.78+11851G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149742271 | |||||||
| chr5:149742418 | T | C | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+11998T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149742418 | |||||||
| chr5:149742591 | A | G | 3 | a0001c0006t0001g0316 a0007c0019t0017g0314 a0007c0019t0017g0315 |
3 | HG03225.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.78+12171A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149742591 | |||||||
| chr5:149742778 | A | T | 2 | a0005c0026t0034g0310 a0010c0021t0061g0311 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.78+12358A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149742778 | |||||||
| chr5:149742955 | A | G | 58 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(55): Show |
58 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.78+12535A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149742955 | |||||||
| chr5:149743021 | T | G | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+12601T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743021 | |||||||
| chr5:149743155 | C | CT | 13 | a0001c0001t0001g0083 a0001c0001t0001g0228 a0001c0001t0001g0233 others(10): Show |
13 | HG02300.hp1 HG02602.hp1 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.78+12753dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149743155 | ||||||
| chr5:149743155 | CT | C | 7 | a0001c0001t0001g0201 a0001c0001t0003g0151 a0001c0001t0023g0203 others(4): Show |
7 | HG02135.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+12753delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149743155 | ||||||
| chr5:149743362 | G | A | 2 | a0004c0005t0001g0121 a0008c0016t0036g0122 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78+12942G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743362 | |||||||
| chr5:149743393 | T | C | 2 | a0001c0001t0003g0170 a0004c0005t0001g0171 |
2 | HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.78+12973T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743393 | |||||||
| chr5:149743569 | A | G | 129 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.78+13149A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743569 | |||||||
| chr5:149743592 | A | G | 58 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(55): Show |
58 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.78+13172A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743592 | |||||||
| chr5:149743648 | C | T | 2 | a0001c0017t0017g0014 a0006c0007t0016g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.78+13228C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743648 | |||||||
| chr5:149743768 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.78+13348C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743768 | |||||||
| chr5:149743882 | C | T | 2 | a0001c0001t0015g0300 a0002c0002t0010g0304 |
2 | HG02735.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.78+13462C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743882 | |||||||
| chr5:149743949 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.78+13529G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149743949 | |||||||
| chr5:149744208 | G | T | 1 | a0015c0029t0008g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+13788G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744208 | |||||||
| chr5:149744358 | G | T | 2 | a0002c0002t0025g0027 a0002c0002t0025g0029 |
2 | HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.78+13938G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744358 | |||||||
| chr5:149744371 | C | G | 58 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(55): Show |
58 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.78+13951C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744371 | |||||||
| chr5:149744371 | C | T | 3 | a0001c0006t0001g0316 a0007c0019t0017g0314 a0007c0019t0017g0315 |
3 | HG03225.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.78+13951C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744371 | |||||||
| chr5:149744377 | C | T | 1 | a0003c0003t0004g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.78+13957C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744377 | |||||||
| chr5:149744473 | A | G | 7 | a0001c0006t0001g0313 a0001c0009t0009g0130 a0002c0008t0005g0129 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+14053A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744473 | |||||||
| chr5:149744542 | C | T | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+14122C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744542 | |||||||
| chr5:149744568 | A | G | 124 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.78+14148A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744568 | |||||||
| chr5:149744665 | A | G | 26 | a0001c0001t0003g0103 a0001c0001t0007g0106 a0001c0004t0006g0095 others(23): Show |
26 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.78+14245A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744665 | |||||||
| chr5:149744680 | A | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.78+14260A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744680 | |||||||
| chr5:149744706 | A | G | 1 | a0001c0001t0023g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.78+14286A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744706 | |||||||
| chr5:149744807 | A | G | 4 | a0001c0001t0002g0134 a0001c0001t0002g0152 a0001c0001t0002g0163 others(1): Show |
4 | HG01081.hp2 HG01261.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+14387A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744807 | |||||||
| chr5:149744856 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.78+14436T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744856 | |||||||
| chr5:149744908 | C | CT | 243 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.78+14506dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149744908 | ||||||
| chr5:149744908 | C | CTT | 6 | a0001c0001t0001g0231 a0001c0001t0002g0268 a0001c0001t0012g0085 others(3): Show |
6 | HG01433.hp2 HG02965.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+14505_78+14506d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149744908 | ||||||
| chr5:149744940 | G | C | 1 | a0003c0003t0004g0281 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.78+14520G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744940 | |||||||
| chr5:149744962 | G | A | 4 | a0004c0005t0001g0245 a0005c0013t0001g0013 a0005c0013t0009g0007 others(1): Show |
4 | HG01258.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+14542G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149744962 | |||||||
| chr5:149745110 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+14690G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149745110 | |||||||
| chr5:149745385 | A | G | 1 | a0004c0005t0022g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.78+14965A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149745385 | |||||||
| chr5:149745432 | G | A | 36 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(33): Show |
36 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.78+15012G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149745432 | |||||||
| chr5:149745500 | G | A | 2 | a0005c0026t0034g0310 a0010c0021t0061g0311 |
2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.78+15080G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149745500 | |||||||
| chr5:149745755 | TG | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0201 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.78+15336delG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149745755 | |||||||
| chr5:149745796 | C | T | 1 | a0001c0010t0001g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.78+15376C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149745796 | |||||||
| chr5:149745886 | T | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0201 others(74): Show |
77 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.78+15466T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149745886 | |||||||
| chr5:149745930 | A | G | 1 | a0003c0012t0014g0120 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.78+15510A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149745930 | |||||||
| chr5:149746132 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+15712G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149746132 | |||||||
| chr5:149746158 | C | G | 39 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(36): Show |
39 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.78+15738C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149746158 | |||||||
| chr5:149746188 | C | G | 1 | a0001c0004t0018g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.78+15768C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149746188 | |||||||
| chr5:149746207 | C | T | 1 | a0001c0001t0019g0082 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.78+15787C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149746207 | |||||||
| chr5:149746275 | C | T | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.78+15855C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149746275 | |||||||
| chr5:149746981 | T | C | 1 | a0001c0004t0018g0034 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+16561T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149746981 | |||||||
| chr5:149747117 | A | G | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+16697A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149747117 | |||||||
| chr5:149747118 | T | G | 1 | a0001c0001t0003g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.78+16698T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149747118 | |||||||
| chr5:149747423 | C | A | 6 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0002g0205 others(3): Show |
6 | NA18962.hp1 NA18981.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+17003C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149747423 | |||||||
| chr5:149747434 | G | A | 8 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0057g0238 others(5): Show |
8 | HG01106.hp1 HG01346.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+17014G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149747434 | |||||||
| chr5:149747993 | G | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.78+17573G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149747993 | |||||||
| chr5:149748286 | G | GAGATAT | 13 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0002g0154 others(10): Show |
13 | HG00408.hp2 HG00558.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.78+17898_78+17903d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149748286 | ||||||
| chr5:149748286 | G | GAGATATA others(5): Show |
3 | a0001c0010t0056g0153 a0003c0003t0004g0247 a0004c0005t0001g0246 |
3 | HG02630.hp1 NA18980.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.78+17892_78+17903d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149748286 | ||||||
| chr5:149748286 | G | GAGATATA others(11): Show |
1 | a0004c0005t0001g0121 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.78+17886_78+17903d others(20): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149748286 | ||||||
| chr5:149748286 | GAGATAT | G | 57 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0001t0001g0285 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.78+17898_78+17903d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149748286 | ||||||
| chr5:149748286 | GAGATATA others(5): Show |
G | 1 | a0001c0001t0002g0227 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.78+17892_78+17903d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149748286 | ||||||
| chr5:149748314 | TATAG | T | 109 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.78+17898_78+17901d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149748314 | ||||||
| chr5:149748321 | A | C | 2 | a0001c0010t0009g0036 a0006c0007t0016g0035 |
2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.78+17901A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149748321 | |||||||
| chr5:149748323 | A | C | 109 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.78+17903A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149748323 | |||||||
| chr5:149748325 | C | A | 111 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.78+17905C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149748325 | |||||||
| chr5:149748325 | C | CTA | 3 | a0001c0004t0006g0102 a0002c0002t0005g0059 a0002c0002t0008g0030 |
3 | HG01168.hp1 HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.78+17917_78+17918d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149748325 | ||||||
| chr5:149748417 | T | A | 1 | a0001c0001t0012g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.78+17997T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149748417 | |||||||
| chr5:149748758 | C | T | 1 | a0001c0001t0003g0182 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.78+18338C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149748758 | |||||||
| chr5:149748808 | C | T | 1 | a0001c0001t0003g0273 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.78+18388C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149748808 | |||||||
| chr5:149748879 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.78+18459G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149748879 | |||||||
| chr5:149748989 | A | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.78+18569A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149748989 | |||||||
| chr5:149749045 | GT | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.78+18627delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149749045 | ||||||
| chr5:149749141 | C | A | 1 | a0001c0006t0001g0099 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78+18721C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749141 | |||||||
| chr5:149749207 | A | G | 11 | a0001c0004t0024g0077 a0001c0004t0024g0080 a0001c0010t0001g0056 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.78+18787A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749207 | |||||||
| chr5:149749361 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0020g0126 |
3 | NA18945.hp1 NA18990.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.78+18941C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749361 | |||||||
| chr5:149749440 | T | A | 35 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+19020T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749440 | |||||||
| chr5:149749462 | C | T | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.78+19042C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749462 | |||||||
| chr5:149749586 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.78+19166C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749586 | |||||||
| chr5:149749756 | G | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+19336G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749756 | |||||||
| chr5:149749794 | G | C | 1 | a0002c0008t0063g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.78+19374G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749794 | |||||||
| chr5:149749824 | G | A | 1 | a0001c0004t0006g0210 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.78+19404G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749824 | |||||||
| chr5:149749825 | T | G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.78+19405T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749825 | |||||||
| chr5:149749834 | T | C | 1 | a0001c0018t0058g0211 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.78+19414T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749834 | |||||||
| chr5:149749923 | A | G | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+19503A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149749923 | |||||||
| chr5:149750365 | T | TTCCACAG others(10): Show |
1 | a0001c0001t0001g0061 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.78+19951_78+19967d others(19): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750365 | ||||||
| chr5:149750410 | A | G | 2 | a0001c0001t0045g0198 a0004c0015t0001g0196 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.78+19990A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750410 | |||||||
| chr5:149750449 | T | TATATATA others(16): Show |
1 | a0001c0001t0002g0154 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.78+20029_78+20030i others(25): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750449 | |||||||
| chr5:149750451 | A | AATATATA others(19): Show |
1 | a0001c0001t0002g0173 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.78+20032_78+20033i others(28): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750451 | ||||||
| chr5:149750451 | AAAATATA others(7): Show |
A | 6 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+20033_78+20046d others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750451 | ||||||
| chr5:149750451 | AAAATATA others(9): Show |
A | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.78+20033_78+20048d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750451 | ||||||
| chr5:149750453 | A | AATATAT | 3 | a0001c0001t0070g0144 a0001c0004t0024g0037 a0002c0014t0005g0017 |
3 | HG02486.hp1 HG03453.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.78+20064_78+20069d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(1): Show |
7 | a0001c0001t0001g0181 a0001c0001t0003g0020 a0001c0001t0003g0057 others(4): Show |
7 | HG00609.hp2 HG00738.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+20062_78+20069d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(3): Show |
8 | a0001c0001t0001g0155 a0001c0001t0001g0165 a0001c0006t0001g0099 others(5): Show |
8 | HG03139.hp2 NA18941.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+20060_78+20069d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(5): Show |
7 | a0001c0001t0001g0186 a0001c0001t0003g0024 a0001c0001t0003g0026 others(4): Show |
7 | HG01081.hp1 HG02040.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+20058_78+20069d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(7): Show |
4 | a0001c0001t0007g0025 a0001c0006t0042g0001 a0002c0002t0025g0027 others(1): Show |
4 | HG01106.hp2 HG01496.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+20056_78+20069d others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(9): Show |
1 | a0001c0010t0056g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.78+20054_78+20069d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(11): Show |
6 | a0001c0001t0001g0149 a0001c0001t0003g0022 a0001c0001t0021g0146 others(3): Show |
6 | HG00099.hp2 HG01891.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+20052_78+20069d others(20): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(13): Show |
5 | a0001c0001t0003g0135 a0001c0001t0003g0158 a0002c0008t0008g0191 others(2): Show |
5 | HG02071.hp1 HG02083.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.78+20050_78+20069d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(15): Show |
7 | a0001c0001t0002g0164 a0001c0001t0003g0044 a0001c0001t0003g0156 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+20048_78+20069d others(24): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(17): Show |
14 | a0001c0001t0001g0190 a0001c0001t0002g0134 a0001c0001t0002g0163 others(11): Show |
14 | HG00558.hp1 HG01261.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+20046_78+20069d others(26): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(19): Show |
7 | a0001c0001t0002g0148 a0001c0001t0003g0123 a0001c0001t0003g0160 others(4): Show |
7 | HG01175.hp2 HG02523.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+20044_78+20069d others(28): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(21): Show |
7 | a0001c0001t0001g0161 a0001c0001t0001g0312 a0001c0001t0003g0172 others(4): Show |
7 | HG00408.hp2 HG00741.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+20042_78+20069d others(30): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(23): Show |
1 | a0001c0001t0003g0167 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.78+20040_78+20069d others(32): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(25): Show |
1 | a0001c0001t0002g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.78+20038_78+20069d others(34): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | AATATATA others(27): Show |
1 | a0001c0001t0003g0182 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.78+20036_78+20069d others(36): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | A | ATATATAT others(10): Show |
1 | a0001c0010t0038g0185 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.78+20033_78+20034i others(19): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750453 | |||||||
| chr5:149750453 | A | ATATATAT others(30): Show |
1 | a0001c0001t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.78+20033_78+20034i others(39): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750453 | |||||||
| chr5:149750453 | A | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0173 |
2 | NA19084.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.78+20033A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750453 | |||||||
| chr5:149750453 | AATAT | A | 4 | a0001c0001t0039g0141 a0001c0001t0051g0145 a0001c0009t0023g0218 others(1): Show |
4 | HG01943.hp2 HG03491.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+20066_78+20069d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | AATATAT | A | 9 | a0001c0001t0001g0143 a0001c0001t0002g0208 a0001c0001t0009g0142 others(6): Show |
9 | HG01074.hp2 HG01934.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.78+20064_78+20069d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | AATATATA others(1): Show |
A | 15 | a0001c0001t0001g0201 a0001c0001t0001g0233 a0001c0001t0001g0258 others(12): Show |
15 | HG01255.hp2 HG01928.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.78+20062_78+20069d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | AATATATA others(3): Show |
A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0206 a0001c0001t0001g0207 others(56): Show |
59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.78+20060_78+20069d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | AATATATA others(5): Show |
A | 39 | a0001c0001t0001g0047 a0001c0001t0001g0228 a0001c0001t0001g0285 others(36): Show |
39 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.78+20058_78+20069d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | AATATATA others(7): Show |
A | 59 | a0001c0001t0001g0010 a0001c0001t0001g0053 a0001c0001t0001g0061 others(56): Show |
59 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.78+20056_78+20069d others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | AATATATA others(9): Show |
A | 9 | a0001c0006t0001g0316 a0001c0009t0064g0261 a0001c0022t0006g0097 others(6): Show |
9 | HG00735.hp2 HG02451.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.78+20054_78+20069d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | AATATATA others(11): Show |
A | 27 | a0001c0001t0002g0307 a0001c0001t0003g0103 a0001c0001t0007g0106 others(24): Show |
27 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.78+20052_78+20069d others(20): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750453 | AATATATA others(13): Show |
A | 2 | a0001c0004t0018g0031 a0004c0005t0001g0171 |
2 | HG02135.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.78+20050_78+20069d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149750453 | ||||||
| chr5:149750461 | T | A | 1 | a0002c0002t0032g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.78+20041T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750461 | |||||||
| chr5:149750463 | T | A | 1 | a0002c0002t0032g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.78+20043T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750463 | |||||||
| chr5:149750465 | T | A | 1 | a0002c0002t0032g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.78+20045T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750465 | |||||||
| chr5:149750567 | A | G | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+20147A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750567 | |||||||
| chr5:149750769 | G | A | 1 | a0001c0001t0003g0103 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.78+20349G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750769 | |||||||
| chr5:149750794 | G | A | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+20374G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750794 | |||||||
| chr5:149750907 | T | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0047 others(195): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.78+20487T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149750907 | |||||||
| chr5:149751003 | T | TTTATA | 182 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0047 others(179): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.78+20586_78+20587i others(7): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149751003 | ||||||
| chr5:149751085 | CCTTTTA | C | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+20672_78+20677d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149751085 | ||||||
| chr5:149751215 | C | G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.78+20795C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751215 | |||||||
| chr5:149751359 | T | C | 1 | a0001c0004t0018g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.78+20939T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751359 | |||||||
| chr5:149751359 | T | G | 3 | a0004c0005t0001g0121 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78+20939T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751359 | |||||||
| chr5:149751428 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(72): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.78+21008G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751428 | |||||||
| chr5:149751460 | C | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(72): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.78+21040C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751460 | |||||||
| chr5:149751477 | G | A | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.78+21057G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751477 | |||||||
| chr5:149751481 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.78+21061G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751481 | |||||||
| chr5:149751534 | C | T | 91 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.78+21114C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751534 | |||||||
| chr5:149751633 | G | A | 27 | a0001c0001t0002g0307 a0001c0001t0003g0103 a0001c0001t0007g0106 others(24): Show |
27 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.78+21213G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751633 | |||||||
| chr5:149751708 | A | G | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+21288A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751708 | |||||||
| chr5:149751709 | GA | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+21302delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149751709 | ||||||
| chr5:149751716 | A | G | 1 | a0001c0001t0003g0156 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.78+21296A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751716 | |||||||
| chr5:149751805 | C | G | 13 | a0001c0001t0015g0289 a0001c0001t0020g0299 a0003c0003t0004g0281 others(10): Show |
13 | HG01433.hp1 HG01496.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+21385C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751805 | |||||||
| chr5:149751810 | C | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0190 others(1): Show |
4 | HG00558.hp1 NA18943.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+21390C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751810 | |||||||
| chr5:149751908 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+21488G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751908 | |||||||
| chr5:149751982 | A | G | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+21562A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149751982 | |||||||
| chr5:149752294 | A | G | 1 | a0001c0001t0002g0307 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.78+21874A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752294 | |||||||
| chr5:149752380 | G | A | 2 | a0001c0004t0018g0034 a0001c0004t0018g0039 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.78+21960G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752380 | |||||||
| chr5:149752391 | G | T | 1 | a0002c0002t0005g0016 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.78+21971G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752391 | |||||||
| chr5:149752779 | A | T | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22359A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752779 | |||||||
| chr5:149752782 | T | C | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22362T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752782 | |||||||
| chr5:149752783 | C | T | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22363C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752783 | |||||||
| chr5:149752786 | A | G | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22366A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752786 | |||||||
| chr5:149752787 | C | T | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22367C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752787 | |||||||
| chr5:149752790 | T | C | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22370T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752790 | |||||||
| chr5:149752800 | G | A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22380G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752800 | |||||||
| chr5:149752802 | C | T | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22382C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752802 | |||||||
| chr5:149752804 | G | A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+22384G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752804 | |||||||
| chr5:149752983 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+22563A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752983 | |||||||
| chr5:149752990 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+22570A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149752990 | |||||||
| chr5:149753025 | T | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0201 others(75): Show |
78 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.78+22605T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753025 | |||||||
| chr5:149753027 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.78+22607C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753027 | |||||||
| chr5:149753103 | G | T | 1 | a0002c0002t0008g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.78+22683G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753103 | |||||||
| chr5:149753105 | A | T | 1 | a0002c0002t0008g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.78+22685A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753105 | |||||||
| chr5:149753238 | G | A | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+22818G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753238 | |||||||
| chr5:149753241 | C | G | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.78+22821C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753241 | |||||||
| chr5:149753460 | G | A | 1 | a0001c0004t0024g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.78+23040G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753460 | |||||||
| chr5:149753541 | T | A | 8 | a0001c0006t0001g0199 a0001c0006t0001g0209 a0001c0006t0001g0313 others(5): Show |
8 | HG01243.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+23121T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753541 | |||||||
| chr5:149753658 | G | T | 1 | a0001c0001t0002g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.78+23238G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753658 | |||||||
| chr5:149753899 | G | A | 4 | a0002c0002t0005g0006 a0002c0002t0008g0003 a0009c0020t0008g0004 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+23479G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753899 | |||||||
| chr5:149753983 | C | T | 3 | a0004c0005t0001g0121 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78+23563C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149753983 | |||||||
| chr5:149754037 | T | C | 1 | a0001c0001t0050g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.78+23617T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754037 | |||||||
| chr5:149754171 | A | G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.78+23751A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754171 | |||||||
| chr5:149754174 | G | T | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.78+23754G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754174 | |||||||
| chr5:149754277 | C | G | 1 | a0001c0001t0012g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.78+23857C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754277 | |||||||
| chr5:149754310 | C | T | 2 | a0001c0001t0003g0170 a0004c0005t0001g0171 |
2 | HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.78+23890C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754310 | |||||||
| chr5:149754310 | CG | C | 26 | a0001c0001t0002g0307 a0001c0001t0003g0103 a0001c0001t0007g0106 others(23): Show |
26 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.78+23891delG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754310 | |||||||
| chr5:149754311 | G | A | 92 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.78+23891G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754311 | |||||||
| chr5:149754311 | G | T | 1 | a0001c0004t0006g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.78+23891G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754311 | |||||||
| chr5:149754312 | T | G | 1 | a0001c0004t0006g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.78+23892T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754312 | |||||||
| chr5:149754313 | G | C | 1 | a0001c0004t0006g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.78+23893G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754313 | |||||||
| chr5:149754418 | A | T | 1 | a0001c0001t0012g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.78+23998A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754418 | |||||||
| chr5:149754644 | G | A | 7 | a0001c0006t0001g0316 a0001c0009t0064g0261 a0001c0030t0031g0320 others(4): Show |
7 | HG02451.hp1 HG03041.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+24224G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754644 | |||||||
| chr5:149754647 | C | T | 7 | a0001c0006t0001g0316 a0001c0009t0064g0261 a0001c0030t0031g0320 others(4): Show |
7 | HG02451.hp1 HG03041.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+24227C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754647 | |||||||
| chr5:149754654 | G | A | 1 | a0001c0004t0006g0277 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.78+24234G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754654 | |||||||
| chr5:149754771 | C | G | 1 | a0001c0001t0003g0151 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.78+24351C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754771 | |||||||
| chr5:149754774 | A | AT | 8 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0007g0025 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+24380dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149754774 | ||||||
| chr5:149754774 | AT | A | 140 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0098 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.78+24380delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149754774 | ||||||
| chr5:149754774 | ATT | A | 31 | a0001c0001t0001g0143 a0001c0001t0001g0155 a0001c0001t0001g0161 others(28): Show |
31 | HG00558.hp1 HG00741.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.78+24379_78+24380d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149754774 | ||||||
| chr5:149754774 | ATTT | A | 58 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0002g0307 others(55): Show |
58 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.78+24378_78+24380d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149754774 | ||||||
| chr5:149754912 | A | G | 33 | a0001c0001t0001g0233 a0001c0001t0001g0240 a0001c0001t0001g0242 others(30): Show |
33 | HG00558.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.78+24492A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754912 | |||||||
| chr5:149754996 | T | G | 1 | a0001c0001t0012g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.78+24576T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149754996 | |||||||
| chr5:149755040 | C | CATATATA others(3): Show |
2 | a0001c0001t0003g0272 a0001c0001t0003g0273 |
2 | NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+24625_78+24626i others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755040 | ||||||
| chr5:149755040 | C | CATATATA others(13): Show |
2 | a0001c0001t0001g0271 a0007c0019t0017g0314 |
2 | HG03831.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.78+24625_78+24626i others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755040 | ||||||
| chr5:149755040 | CATATACA others(9): Show |
C | 35 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+24626_78+24641d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755040 | ||||||
| chr5:149755040 | CATATACA others(13): Show |
C | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.78+24626_78+24645d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755040 | ||||||
| chr5:149755042 | T | TATAC | 34 | a0001c0001t0001g0002 a0001c0001t0001g0230 a0001c0001t0001g0231 others(31): Show |
34 | HG00558.hp2 HG00639.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.78+24626_78+24629d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755042 | ||||||
| chr5:149755046 | C | CATACAT | 3 | a0001c0001t0023g0229 a0001c0010t0001g0255 a0003c0003t0004g0247 |
3 | HG02258.hp1 HG02735.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.78+24629_78+24630i others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755046 | ||||||
| chr5:149755046 | C | CATATAT | 3 | a0001c0001t0001g0018 a0002c0002t0005g0016 a0015c0029t0008g0270 |
3 | NA18522.hp1 NA19012.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.78+24631_78+24632i others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755046 | ||||||
| chr5:149755046 | C | CATATATA others(9): Show |
1 | a0007c0019t0017g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.78+24631_78+24632i others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755046 | ||||||
| chr5:149755046 | C | CATATATA others(11): Show |
3 | a0001c0001t0001g0312 a0001c0006t0001g0316 a0001c0030t0031g0320 |
3 | HG03041.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.78+24631_78+24632i others(20): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755046 | ||||||
| chr5:149755046 | C | CATATATA others(13): Show |
2 | a0005c0026t0034g0310 a0013c0027t0037g0318 |
2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.78+24631_78+24632i others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755046 | ||||||
| chr5:149755046 | C | CATATATA others(15): Show |
1 | a0005c0013t0009g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.78+24631_78+24632i others(24): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755046 | ||||||
| chr5:149755046 | C | T | 4 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 others(1): Show |
4 | HG03831.hp2 HG06807.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+24626C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755046 | |||||||
| chr5:149755046 | CATATACA others(5): Show |
C | 1 | a0002c0002t0005g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.78+24632_78+24643d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755046 | ||||||
| chr5:149755046 | CATATACA others(7): Show |
C | 54 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(51): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.78+24632_78+24645d others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755046 | ||||||
| chr5:149755048 | T | TAC | 9 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0194 others(6): Show |
9 | HG00735.hp1 HG01074.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.78+24629_78+24630i others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755048 | ||||||
| chr5:149755050 | T | C | 32 | a0001c0001t0001g0149 a0001c0001t0001g0201 a0001c0001t0001g0206 others(29): Show |
32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.78+24630T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755050 | |||||||
| chr5:149755052 | C | CAT | 4 | a0001c0006t0001g0099 a0001c0006t0001g0100 a0008c0016t0026g0262 others(1): Show |
4 | HG02647.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+24652_78+24653d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATAT | 17 | a0001c0001t0002g0307 a0001c0004t0006g0095 a0001c0004t0006g0102 others(14): Show |
17 | HG01168.hp1 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.78+24650_78+24653d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATACA others(3): Show |
6 | a0001c0001t0003g0103 a0002c0002t0008g0003 a0004c0005t0022g0109 others(3): Show |
6 | HG00544.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+24637_78+24638i others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATAT | 9 | a0001c0001t0007g0106 a0001c0004t0006g0101 a0001c0004t0006g0112 others(6): Show |
9 | HG00280.hp2 HG01346.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.78+24648_78+24653d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(1): Show |
6 | a0001c0004t0018g0031 a0001c0004t0024g0037 a0006c0007t0016g0035 others(3): Show |
6 | HG02896.hp1 HG02897.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+24646_78+24653d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(3): Show |
6 | a0001c0001t0001g0165 a0001c0004t0018g0034 a0001c0004t0018g0039 others(3): Show |
6 | HG02280.hp1 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+24644_78+24653d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(5): Show |
9 | a0001c0001t0003g0020 a0001c0001t0003g0022 a0001c0001t0003g0024 others(6): Show |
9 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.78+24642_78+24653d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(7): Show |
1 | a0002c0008t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.78+24640_78+24653d others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(9): Show |
1 | a0017c0034t0013g0021 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.78+24638_78+24653d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(11): Show |
2 | a0002c0014t0005g0017 a0002c0014t0005g0019 |
2 | HG00609.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.78+24636_78+24653d others(20): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(13): Show |
1 | a0008c0016t0026g0009 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.78+24634_78+24653d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(15): Show |
1 | a0005c0011t0001g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.78+24653_78+24654i others(24): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(17): Show |
2 | a0002c0008t0008g0319 a0005c0011t0009g0133 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.78+24653_78+24654i others(26): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(19): Show |
8 | a0001c0001t0001g0228 a0001c0009t0009g0130 a0001c0017t0017g0014 others(5): Show |
8 | HG02572.hp1 HG02602.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+24653_78+24654i others(28): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(21): Show |
1 | a0004c0005t0001g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.78+24653_78+24654i others(30): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | CATATATA others(25): Show |
1 | a0001c0001t0001g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.78+24653_78+24654i others(34): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755052 | ||||||
| chr5:149755052 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0149 others(89): Show |
92 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.78+24632C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755052 | |||||||
| chr5:149755057 | A | G | 2 | a0001c0001t0002g0227 a0001c0001t0041g0222 |
2 | HG02132.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.78+24637A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755057 | |||||||
| chr5:149755120 | G | C | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+24700G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755120 | |||||||
| chr5:149755440 | A | G | 2 | a0001c0001t0012g0124 a0001c0001t0012g0162 |
2 | NA18963.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.78+25020A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755440 | |||||||
| chr5:149755443 | C | T | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.78+25023C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755443 | |||||||
| chr5:149755482 | T | C | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+25062T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755482 | |||||||
| chr5:149755562 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+25142G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755562 | |||||||
| chr5:149755597 | GTTA | G | 13 | a0001c0001t0020g0299 a0002c0002t0010g0073 a0003c0003t0004g0281 others(10): Show |
13 | HG01433.hp1 HG01496.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+25192_78+25194d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755597 | ||||||
| chr5:149755597 | GTTATTAT others(17): Show |
G | 3 | a0001c0009t0064g0261 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.78+25195_78+25218d others(26): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755597 | ||||||
| chr5:149755597 | GTTATTAT others(20): Show |
G | 7 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0004c0005t0001g0121 others(4): Show |
7 | HG02451.hp1 HG03041.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+25195_78+25221d others(29): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755597 | ||||||
| chr5:149755600 | A | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0201 others(75): Show |
78 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.78+25180A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755600 | |||||||
| chr5:149755611 | T | C | 1 | a0001c0001t0003g0044 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.78+25191T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755611 | |||||||
| chr5:149755615 | G | GTTA | 3 | a0001c0001t0001g0061 a0002c0002t0008g0030 a0003c0003t0011g0063 |
3 | HG01952.hp1 HG03579.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.78+25225_78+25227d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755615 | ||||||
| chr5:149755615 | GTTA | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0143 others(216): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.78+25225_78+25227d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755615 | ||||||
| chr5:149755615 | GTTATTA | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0186 a0001c0001t0015g0180 others(2): Show |
5 | HG02040.hp2 HG02056.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.78+25222_78+25227d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149755615 | ||||||
| chr5:149755618 | A | G | 12 | a0001c0001t0020g0299 a0003c0003t0004g0281 a0003c0003t0004g0290 others(9): Show |
12 | HG01433.hp1 HG01496.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.78+25198A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755618 | |||||||
| chr5:149755624 | A | G | 1 | a0008c0016t0026g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78+25204A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755624 | |||||||
| chr5:149755642 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.78+25222A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755642 | |||||||
| chr5:149755643 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.78+25223T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755643 | |||||||
| chr5:149755645 | A | G | 1 | a0003c0003t0004g0305 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.78+25225A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755645 | |||||||
| chr5:149755646 | T | C | 1 | a0003c0003t0004g0305 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.78+25226T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755646 | |||||||
| chr5:149755706 | C | T | 89 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.78+25286C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755706 | |||||||
| chr5:149755746 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+25326C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755746 | |||||||
| chr5:149755850 | G | A | 1 | a0001c0001t0044g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.78+25430G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755850 | |||||||
| chr5:149755895 | T | C | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.78+25475T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755895 | |||||||
| chr5:149755913 | G | A | 1 | a0002c0002t0008g0003 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.78+25493G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755913 | |||||||
| chr5:149755939 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+25519C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149755939 | |||||||
| chr5:149756061 | CT | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+25642delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756061 | |||||||
| chr5:149756159 | A | T | 33 | a0001c0001t0001g0233 a0001c0001t0001g0240 a0001c0001t0001g0242 others(30): Show |
33 | HG00558.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.78+25739A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756159 | |||||||
| chr5:149756233 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03831.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.78+25813G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756233 | |||||||
| chr5:149756324 | C | G | 1 | a0003c0003t0004g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.78+25904C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756324 | |||||||
| chr5:149756344 | T | G | 2 | a0008c0016t0026g0262 a0008c0016t0036g0122 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.78+25924T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756344 | |||||||
| chr5:149756367 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.78+25947A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756367 | |||||||
| chr5:149756377 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.78+25957A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756377 | |||||||
| chr5:149756409 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.78+25989G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756409 | |||||||
| chr5:149756776 | G | A | 1 | a0001c0001t0051g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.78+26356G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756776 | |||||||
| chr5:149756869 | T | A | 1 | a0004c0015t0001g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.78+26449T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756869 | |||||||
| chr5:149756893 | G | T | 3 | a0004c0005t0001g0121 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78+26473G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756893 | |||||||
| chr5:149756993 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.78+26573G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149756993 | |||||||
| chr5:149757069 | T | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0053 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.78+26649T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757069 | |||||||
| chr5:149757099 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0053 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.78+26679G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757099 | |||||||
| chr5:149757249 | A | T | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+26829A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757249 | |||||||
| chr5:149757286 | C | CA | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+26869dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149757286 | ||||||
| chr5:149757348 | A | G | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+26928A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757348 | |||||||
| chr5:149757348 | AT | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0149 others(110): Show |
113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.78+26940delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149757348 | ||||||
| chr5:149757360 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0201 others(75): Show |
78 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.78+26940T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757360 | |||||||
| chr5:149757395 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.78+26975A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757395 | |||||||
| chr5:149757473 | A | G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.78+27053A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757473 | |||||||
| chr5:149757557 | C | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0053 others(129): Show |
132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.78+27137C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757557 | |||||||
| chr5:149757561 | C | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0047 others(184): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.78+27141C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757561 | |||||||
| chr5:149757571 | C | T | 1 | a0015c0029t0008g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+27151C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757571 | |||||||
| chr5:149757761 | G | C | 1 | a0001c0001t0028g0214 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.78+27341G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757761 | |||||||
| chr5:149757843 | C | G | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+27423C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757843 | |||||||
| chr5:149757891 | C | A | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+27471C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149757891 | |||||||
| chr5:149758042 | C | G | 2 | a0001c0001t0002g0278 a0001c0004t0006g0277 |
2 | HG00738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.78+27622C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149758042 | |||||||
| chr5:149758061 | C | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(72): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.78+27641C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149758061 | |||||||
| chr5:149758548 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(226): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.78+28128T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149758548 | |||||||
| chr5:149758665 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0053 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.78+28245G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149758665 | |||||||
| chr5:149758692 | C | T | 5 | a0001c0001t0003g0058 a0001c0001t0019g0052 a0001c0001t0019g0072 others(2): Show |
5 | HG00099.hp1 HG01109.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+28272C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149758692 | |||||||
| chr5:149759172 | T | C | 2 | a0002c0008t0008g0191 a0002c0008t0063g0169 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.78+28752T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759172 | |||||||
| chr5:149759262 | G | A | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+28842G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759262 | |||||||
| chr5:149759349 | C | T | 7 | a0001c0001t0001g0143 a0001c0001t0009g0142 a0001c0001t0021g0140 others(4): Show |
7 | HG00741.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+28929C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759349 | |||||||
| chr5:149759503 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.78+29083A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759503 | |||||||
| chr5:149759606 | G | A | 29 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0003g0020 others(26): Show |
29 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.78+29186G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759606 | |||||||
| chr5:149759652 | C | T | 1 | a0004c0005t0001g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.78+29232C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759652 | |||||||
| chr5:149759667 | C | T | 2 | a0001c0018t0029g0197 a0004c0005t0001g0257 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.78+29247C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759667 | |||||||
| chr5:149759704 | G | T | 1 | a0001c0010t0038g0185 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.78+29284G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759704 | |||||||
| chr5:149759798 | C | T | 41 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(38): Show |
41 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.78+29378C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759798 | |||||||
| chr5:149759983 | C | T | 2 | a0001c0001t0001g0070 a0004c0005t0013g0071 |
2 | HG02071.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.78+29563C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149759983 | |||||||
| chr5:149760095 | G | A | 1 | a0001c0001t0040g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.78+29675G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760095 | |||||||
| chr5:149760120 | C | T | 35 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+29700C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760120 | |||||||
| chr5:149760246 | G | C | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+29826G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760246 | |||||||
| chr5:149760337 | A | C | 6 | a0001c0001t0015g0300 a0002c0002t0010g0304 a0002c0002t0025g0286 others(3): Show |
6 | HG00140.hp2 HG01943.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+29917A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760337 | |||||||
| chr5:149760381 | C | G | 1 | a0001c0004t0018g0034 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+29961C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760381 | |||||||
| chr5:149760412 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+29992C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760412 | |||||||
| chr5:149760513 | A | G | 7 | a0001c0001t0001g0312 a0001c0009t0064g0261 a0002c0002t0005g0006 others(4): Show |
7 | HG02451.hp2 HG02922.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+30093A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760513 | |||||||
| chr5:149760593 | G | T | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+30173G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760593 | |||||||
| chr5:149760603 | G | A | 1 | a0001c0001t0002g0173 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.78+30183G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760603 | |||||||
| chr5:149760699 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.78+30279A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760699 | |||||||
| chr5:149760737 | C | T | 256 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.78+30317C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760737 | |||||||
| chr5:149760796 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.78+30376A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760796 | |||||||
| chr5:149760847 | G | A | 1 | a0001c0009t0002g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.78+30427G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760847 | |||||||
| chr5:149760987 | C | T | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.78+30567C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149760987 | |||||||
| chr5:149761004 | G | A | 1 | a0002c0002t0032g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.78+30584G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761004 | |||||||
| chr5:149761079 | T | C | 2 | a0001c0001t0001g0233 a0001c0001t0015g0232 |
2 | NA18948.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.78+30659T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761079 | |||||||
| chr5:149761194 | A | G | 7 | a0001c0001t0001g0312 a0001c0009t0064g0261 a0002c0002t0005g0006 others(4): Show |
7 | HG02451.hp2 HG02922.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+30774A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761194 | |||||||
| chr5:149761219 | C | A | 3 | a0001c0006t0001g0316 a0007c0019t0017g0314 a0007c0019t0017g0315 |
3 | HG03225.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.78+30799C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761219 | |||||||
| chr5:149761223 | A | G | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.78+30803A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761223 | |||||||
| chr5:149761300 | T | C | 33 | a0001c0001t0001g0233 a0001c0001t0001g0240 a0001c0001t0001g0242 others(30): Show |
33 | HG00558.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.78+30880T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761300 | |||||||
| chr5:149761427 | T | C | 62 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0165 others(59): Show |
62 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.78+31007T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761427 | |||||||
| chr5:149761470 | T | A | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.78+31050T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761470 | |||||||
| chr5:149761743 | GTGATGT | G | 6 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0007c0019t0017g0314 others(3): Show |
6 | HG02451.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+31325_78+31330d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149761743 | ||||||
| chr5:149761846 | G | C | 35 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0003g0020 others(32): Show |
35 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+31426G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761846 | |||||||
| chr5:149761854 | C | T | 2 | a0008c0016t0026g0262 a0008c0016t0036g0122 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.78+31434C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761854 | |||||||
| chr5:149761986 | T | C | 1 | a0004c0005t0013g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.78+31566T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149761986 | |||||||
| chr5:149762155 | G | GT | 34 | a0001c0001t0001g0149 a0001c0001t0001g0228 a0001c0001t0002g0154 others(31): Show |
34 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.78+31752dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149762155 | ||||||
| chr5:149762155 | G | GTTT | 6 | a0001c0009t0064g0261 a0002c0002t0005g0006 a0002c0002t0008g0003 others(3): Show |
6 | HG02451.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+31750_78+31752d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149762155 | ||||||
| chr5:149762155 | GT | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(72): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.78+31752delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149762155 | ||||||
| chr5:149762156 | T | G | 2 | a0002c0002t0025g0027 a0002c0002t0025g0029 |
2 | HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.78+31736T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149762156 | |||||||
| chr5:149762189 | C | G | 1 | a0001c0017t0017g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.78+31769C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149762189 | |||||||
| chr5:149762225 | T | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.78+31805T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149762225 | |||||||
| chr5:149762405 | C | T | 6 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0007c0019t0017g0314 others(3): Show |
6 | HG02451.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+31985C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149762405 | |||||||
| chr5:149762504 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(10): Show |
13 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+32084G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149762504 | |||||||
| chr5:149762522 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.78+32102T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149762522 | |||||||
| chr5:149762753 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(226): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.78+32333T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149762753 | |||||||
| chr5:149762776 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(72): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.78+32356C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149762776 | |||||||
| chr5:149763146 | TTCCCTCC others(19): Show |
T | 27 | a0001c0001t0002g0307 a0001c0001t0003g0103 a0001c0001t0007g0106 others(24): Show |
27 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.78+32729_78+32754d others(28): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149763146 | ||||||
| chr5:149763155 | C | G | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.78+32735C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149763155 | |||||||
| chr5:149763174 | C | T | 4 | a0001c0001t0003g0026 a0002c0002t0010g0038 a0002c0002t0032g0041 others(1): Show |
4 | NA18941.hp2 NA18994.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+32754C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149763174 | |||||||
| chr5:149763204 | C | T | 7 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+32784C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149763204 | |||||||
| chr5:149763334 | G | A | 3 | a0004c0005t0001g0121 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78+32914G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149763334 | |||||||
| chr5:149763526 | G | GT | 15 | a0001c0001t0001g0149 a0001c0001t0001g0190 a0001c0001t0001g0228 others(12): Show |
15 | HG01175.hp2 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.78+33130dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149763526 | ||||||
| chr5:149763526 | GT | G | 75 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0220 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.78+33130delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149763526 | ||||||
| chr5:149763526 | GTT | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0047 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.78+33129_78+33130d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149763526 | ||||||
| chr5:149763526 | GTTT | G | 6 | a0001c0006t0001g0316 a0001c0017t0006g0078 a0001c0030t0031g0320 others(3): Show |
6 | HG02451.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+33128_78+33130d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149763526 | ||||||
| chr5:149763526 | GTTTTTTT others(6): Show |
G | 1 | a0003c0012t0014g0120 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.78+33118_78+33130d others(15): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149763526 | ||||||
| chr5:149763861 | G | A | 4 | a0001c0001t0003g0026 a0002c0002t0010g0038 a0002c0002t0032g0041 others(1): Show |
4 | NA18941.hp2 NA18994.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+33441G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149763861 | |||||||
| chr5:149763950 | G | T | 2 | a0002c0002t0005g0266 a0002c0002t0005g0267 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.78+33530G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149763950 | |||||||
| chr5:149764053 | A | G | 6 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0007c0019t0017g0314 others(3): Show |
6 | HG02451.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+33633A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149764053 | |||||||
| chr5:149764136 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.78+33716A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149764136 | |||||||
| chr5:149764160 | TATAG | T | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+33746_78+33749d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149764160 | ||||||
| chr5:149764189 | G | C | 34 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0003g0020 others(31): Show |
34 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.78+33769G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149764189 | |||||||
| chr5:149764334 | C | T | 1 | a0001c0001t0012g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.78+33914C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149764334 | |||||||
| chr5:149764392 | T | C | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+33972T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149764392 | |||||||
| chr5:149764400 | G | A | 29 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0003g0020 others(26): Show |
29 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.78+33980G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149764400 | |||||||
| chr5:149764533 | GAC | G | 6 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0002g0205 others(3): Show |
6 | NA18962.hp1 NA18981.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+34117_78+34118d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149764533 | ||||||
| chr5:149764956 | CTACCAAC others(103): Show |
C | 14 | a0001c0001t0001g0018 a0001c0001t0003g0020 a0001c0001t0003g0022 others(11): Show |
14 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+34622_78+34731d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149764956 | ||||||
| chr5:149765072 | A | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(10): Show |
13 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+34652A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765072 | |||||||
| chr5:149765101 | T | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0053 others(127): Show |
130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.78+34681T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765101 | |||||||
| chr5:149765124 | C | A | 1 | a0002c0002t0010g0204 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.78+34704C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765124 | |||||||
| chr5:149765164 | G | A | 3 | a0004c0005t0001g0121 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78+34744G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765164 | |||||||
| chr5:149765252 | C | T | 2 | a0001c0018t0029g0197 a0004c0005t0001g0257 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.78+34832C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765252 | |||||||
| chr5:149765306 | G | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.78+34886G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765306 | |||||||
| chr5:149765753 | C | T | 3 | a0001c0004t0006g0112 a0001c0004t0006g0115 a0001c0004t0030g0113 |
3 | HG00280.hp2 HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.78+35333C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765753 | |||||||
| chr5:149765764 | G | A | 11 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0001g0244 others(8): Show |
11 | HG00558.hp2 HG01106.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.78+35344G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765764 | |||||||
| chr5:149765843 | A | T | 1 | a0001c0001t0001g0233 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.78+35423A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765843 | |||||||
| chr5:149765847 | T | C | 55 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0165 others(52): Show |
55 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.78+35427T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765847 | |||||||
| chr5:149765856 | G | A | 1 | a0001c0018t0029g0197 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.78+35436G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149765856 | |||||||
| chr5:149765860 | C | CA | 10 | a0001c0001t0002g0134 a0001c0001t0002g0164 a0001c0001t0003g0135 others(7): Show |
10 | HG02056.hp1 HG02738.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+35462dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149765860 | ||||||
| chr5:149765860 | CA | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0053 others(175): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.78+35462delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149765860 | ||||||
| chr5:149765860 | CAA | C | 6 | a0001c0001t0001g0271 a0001c0001t0001g0312 a0001c0001t0003g0272 others(3): Show |
6 | HG02735.hp2 HG03831.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+35461_78+35462d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149765860 | ||||||
| chr5:149765860 | CAAAA | C | 27 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0003g0020 others(24): Show |
27 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.78+35459_78+35462d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149765860 | ||||||
| chr5:149766142 | A | T | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78+35722A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766142 | |||||||
| chr5:149766246 | A | T | 22 | a0001c0001t0002g0307 a0001c0001t0003g0103 a0001c0001t0007g0106 others(19): Show |
22 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.78+35826A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766246 | |||||||
| chr5:149766356 | A | G | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78+35936A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766356 | |||||||
| chr5:149766459 | T | C | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.78+36039T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766459 | |||||||
| chr5:149766533 | C | T | 2 | a0001c0010t0038g0185 a0002c0008t0071g0184 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.78+36113C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766533 | |||||||
| chr5:149766559 | G | A | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.78+36139G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766559 | |||||||
| chr5:149766582 | AG | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0165 others(46): Show |
49 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.78+36163delG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766582 | |||||||
| chr5:149766657 | C | A | 1 | a0001c0024t0001g0091 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.78+36237C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766657 | |||||||
| chr5:149766667 | T | C | 1 | a0004c0005t0001g0246 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.78+36247T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766667 | |||||||
| chr5:149766759 | G | T | 29 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0001g0312 others(26): Show |
29 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.78+36339G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766759 | |||||||
| chr5:149766917 | C | A | 4 | a0001c0001t0002g0148 a0001c0001t0007g0175 a0001c0001t0007g0176 others(1): Show |
4 | NA18979.hp1 NA18980.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+36497C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766917 | |||||||
| chr5:149766970 | T | G | 6 | a0001c0009t0064g0261 a0002c0002t0005g0006 a0002c0002t0008g0003 others(3): Show |
6 | HG02451.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+36550T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766970 | |||||||
| chr5:149766972 | C | T | 36 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0001g0312 others(33): Show |
36 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.78+36552C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766972 | |||||||
| chr5:149766996 | G | T | 1 | a0001c0004t0006g0210 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.78+36576G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766996 | |||||||
| chr5:149766999 | G | A | 1 | a0002c0002t0010g0066 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.78+36579G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149766999 | |||||||
| chr5:149767018 | C | T | 1 | a0001c0009t0027g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.78+36598C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149767018 | |||||||
| chr5:149767202 | C | T | 4 | a0002c0002t0005g0006 a0002c0002t0008g0003 a0009c0020t0008g0004 others(1): Show |
4 | HG02451.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+36782C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149767202 | |||||||
| chr5:149767767 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0206 others(72): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.78+37347G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149767767 | |||||||
| chr5:149767836 | T | TG | 8 | a0001c0001t0001g0149 a0001c0001t0007g0187 a0001c0004t0006g0101 others(5): Show |
8 | HG01175.hp1 HG02071.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+37422dupG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149767836 | ||||||
| chr5:149767887 | A | G | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.78+37467A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149767887 | |||||||
| chr5:149767980 | C | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(10): Show |
13 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+37560C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149767980 | |||||||
| chr5:149768118 | G | A | 1 | a0001c0001t0007g0215 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78+37698G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768118 | |||||||
| chr5:149768370 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.78+37950G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768370 | |||||||
| chr5:149768409 | G | A | 4 | a0001c0010t0001g0056 a0002c0002t0008g0055 a0005c0011t0009g0054 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+37989G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768409 | |||||||
| chr5:149768441 | A | AT | 15 | a0001c0001t0001g0047 a0001c0001t0001g0092 a0001c0001t0001g0230 others(12): Show |
15 | HG00438.hp1 HG00544.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.78+38041dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149768441 | ||||||
| chr5:149768441 | A | ATT | 27 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0003g0020 others(24): Show |
27 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.78+38040_78+38041d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149768441 | ||||||
| chr5:149768441 | A | ATTT | 11 | a0001c0001t0001g0312 a0001c0009t0064g0261 a0002c0002t0005g0006 others(8): Show |
11 | HG02451.hp2 HG02647.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.78+38039_78+38041d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149768441 | ||||||
| chr5:149768441 | AT | A | 41 | a0001c0001t0001g0149 a0001c0001t0002g0205 a0001c0001t0002g0282 others(38): Show |
41 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.78+38041delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149768441 | ||||||
| chr5:149768441 | ATTTT | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+38038_78+38041d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149768441 | ||||||
| chr5:149768483 | G | A | 6 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0007c0019t0017g0314 others(3): Show |
6 | HG02451.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+38063G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768483 | |||||||
| chr5:149768512 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.78+38092C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768512 | |||||||
| chr5:149768539 | G | A | 3 | a0004c0005t0001g0121 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78+38119G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768539 | |||||||
| chr5:149768548 | ATTCTGCC others(65): Show |
A | 6 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0007c0019t0017g0314 others(3): Show |
6 | HG02451.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+38164_78+38235d others(74): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149768548 | ||||||
| chr5:149768597 | C | G | 3 | a0001c0001t0001g0067 a0001c0001t0002g0050 a0016c0032t0069g0127 |
3 | HG00438.hp1 HG02056.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.78+38177C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768597 | |||||||
| chr5:149768600 | C | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0165 others(46): Show |
49 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.78+38180C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768600 | |||||||
| chr5:149768602 | TCTGGCTA others(65): Show |
T | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+38204_78+38275d others(74): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149768602 | ||||||
| chr5:149768608 | T | C | 6 | a0001c0009t0064g0261 a0002c0002t0005g0006 a0002c0002t0008g0003 others(3): Show |
6 | HG02451.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+38188T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768608 | |||||||
| chr5:149768634 | G | A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+38214G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768634 | |||||||
| chr5:149768752 | G | A | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.78+38332G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768752 | |||||||
| chr5:149768939 | G | A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.78+38519G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768939 | |||||||
| chr5:149768975 | A | G | 1 | a0004c0015t0001g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.78+38555A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149768975 | |||||||
| chr5:149769047 | A | T | 6 | a0001c0006t0001g0316 a0001c0030t0031g0320 a0007c0019t0017g0314 others(3): Show |
6 | HG02451.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+38627A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769047 | |||||||
| chr5:149769117 | G | A | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78+38697G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769117 | |||||||
| chr5:149769159 | G | C | 2 | a0001c0001t0001g0233 a0001c0001t0015g0232 |
2 | NA18948.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.78+38739G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769159 | |||||||
| chr5:149769475 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.78+39055C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769475 | |||||||
| chr5:149769545 | C | T | 11 | a0001c0001t0001g0165 a0001c0004t0018g0031 a0001c0004t0018g0034 others(8): Show |
11 | HG02280.hp1 HG02809.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.78+39125C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769545 | |||||||
| chr5:149769547 | C | T | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.78+39127C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769547 | |||||||
| chr5:149769563 | T | C | 27 | a0001c0001t0002g0307 a0001c0001t0003g0103 a0001c0001t0007g0106 others(24): Show |
27 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.78+39143T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769563 | |||||||
| chr5:149769835 | GCCCTGA | G | 14 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0244 others(11): Show |
14 | HG00558.hp2 HG02040.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+39432_78+39437d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149769835 | ||||||
| chr5:149769849 | C | A | 1 | a0001c0001t0002g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.78+39429C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769849 | |||||||
| chr5:149769913 | G | A | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.78+39493G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769913 | |||||||
| chr5:149769996 | A | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.78+39576A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149769996 | |||||||
| chr5:149770152 | T | A | 3 | a0001c0030t0031g0320 a0013c0027t0037g0318 a0014c0025t0031g0043 |
3 | HG02451.hp1 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.78+39732T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149770152 | |||||||
| chr5:149770155 | T | C | 3 | a0001c0030t0031g0320 a0013c0027t0037g0318 a0014c0025t0031g0043 |
3 | HG02451.hp1 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.78+39735T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149770155 | |||||||
| chr5:149770406 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.78+39986G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149770406 | |||||||
| chr5:149770670 | C | CA | 6 | a0001c0001t0003g0273 a0001c0004t0006g0105 a0001c0006t0001g0199 others(3): Show |
6 | HG01496.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+40263dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149770670 | ||||||
| chr5:149770801 | C | T | 2 | a0001c0001t0002g0278 a0001c0004t0006g0277 |
2 | HG00738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.78+40381C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149770801 | |||||||
| chr5:149770828 | TA | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0001t0015g0289 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.78+40421delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149770828 | ||||||
| chr5:149770902 | T | C | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.78+40482T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149770902 | |||||||
| chr5:149770958 | A | G | 3 | a0001c0006t0001g0316 a0007c0019t0017g0314 a0007c0019t0017g0315 |
3 | HG03225.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.78+40538A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149770958 | |||||||
| chr5:149771085 | C | T | 35 | a0001c0001t0003g0103 a0001c0001t0007g0106 a0001c0004t0006g0095 others(32): Show |
35 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+40665C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771085 | |||||||
| chr5:149771104 | G | T | 3 | a0001c0030t0031g0320 a0013c0027t0037g0318 a0014c0025t0031g0043 |
3 | HG02451.hp1 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.78+40684G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771104 | |||||||
| chr5:149771108 | G | A | 146 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0053 others(143): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.78+40688G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771108 | |||||||
| chr5:149771213 | A | G | 1 | a0006c0007t0016g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.78+40793A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771213 | |||||||
| chr5:149771216 | C | T | 5 | a0002c0002t0005g0006 a0002c0002t0005g0212 a0002c0002t0008g0003 others(2): Show |
5 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.78+40796C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771216 | |||||||
| chr5:149771379 | G | A | 1 | a0001c0001t0041g0222 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.78+40959G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771379 | |||||||
| chr5:149771541 | G | T | 1 | a0001c0017t0017g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.78+41121G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771541 | |||||||
| chr5:149771699 | C | T | 2 | a0002c0008t0008g0191 a0002c0008t0063g0169 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.78+41279C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771699 | |||||||
| chr5:149771756 | C | T | 40 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(37): Show |
40 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.78+41336C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771756 | |||||||
| chr5:149771762 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.78+41342A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771762 | |||||||
| chr5:149771787 | C | T | 1 | a0006c0007t0016g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.78+41367C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771787 | |||||||
| chr5:149771885 | A | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0165 others(103): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.78+41465A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771885 | |||||||
| chr5:149771976 | G | C | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.78+41556G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149771976 | |||||||
| chr5:149772042 | G | A | 1 | a0001c0022t0006g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.78+41622G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772042 | |||||||
| chr5:149772049 | G | A | 11 | a0001c0004t0024g0077 a0001c0004t0024g0080 a0001c0010t0001g0056 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.78+41629G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772049 | |||||||
| chr5:149772124 | C | T | 2 | a0002c0008t0008g0191 a0002c0008t0063g0169 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.78+41704C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772124 | |||||||
| chr5:149772144 | G | A | 33 | a0001c0001t0003g0103 a0001c0001t0007g0106 a0001c0004t0006g0095 others(30): Show |
33 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.78+41724G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772144 | |||||||
| chr5:149772172 | G | A | 7 | a0001c0001t0001g0221 a0001c0009t0009g0130 a0002c0008t0005g0129 others(4): Show |
7 | HG00735.hp1 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+41752G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772172 | |||||||
| chr5:149772313 | C | T | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.78+41893C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772313 | |||||||
| chr5:149772499 | C | T | 6 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+42079C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772499 | |||||||
| chr5:149772584 | C | T | 2 | a0001c0004t0006g0095 a0001c0033t0001g0096 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.78+42164C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772584 | |||||||
| chr5:149772623 | G | T | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+42203G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772623 | |||||||
| chr5:149772859 | G | A | 1 | a0001c0001t0019g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.78+42439G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772859 | |||||||
| chr5:149772968 | G | T | 35 | a0001c0001t0003g0103 a0001c0001t0007g0106 a0001c0004t0006g0095 others(32): Show |
35 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+42548G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149772968 | |||||||
| chr5:149773080 | C | T | 54 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(51): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.78+42660C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773080 | |||||||
| chr5:149773128 | C | T | 62 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0155 others(59): Show |
62 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.78+42708C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773128 | |||||||
| chr5:149773197 | T | C | 1 | a0002c0002t0025g0027 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.78+42777T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773197 | |||||||
| chr5:149773442 | G | C | 4 | a0002c0014t0005g0017 a0002c0014t0005g0019 a0002c0014t0005g0259 others(1): Show |
4 | HG00609.hp2 HG02165.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+43022G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773442 | |||||||
| chr5:149773480 | T | C | 41 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0244 others(38): Show |
41 | HG00408.hp2 HG00558.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.78+43060T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773480 | |||||||
| chr5:149773530 | C | T | 62 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0155 others(59): Show |
62 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.78+43110C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773530 | |||||||
| chr5:149773554 | T | C | 1 | a0003c0003t0004g0281 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.78+43134T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773554 | |||||||
| chr5:149773580 | AC | A | 35 | a0001c0001t0003g0103 a0001c0001t0007g0106 a0001c0004t0006g0095 others(32): Show |
35 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+43161delC | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773580 | |||||||
| chr5:149773644 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.78+43224C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773644 | |||||||
| chr5:149773658 | G | T | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.78+43238G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773658 | |||||||
| chr5:149773666 | T | C | 1 | a0008c0016t0036g0122 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.78+43246T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773666 | |||||||
| chr5:149773668 | A | C | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78+43248A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773668 | |||||||
| chr5:149773684 | G | T | 1 | a0001c0001t0041g0222 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.78+43264G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773684 | |||||||
| chr5:149773764 | G | A | 1 | a0001c0001t0012g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.78+43344G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773764 | |||||||
| chr5:149773966 | A | T | 3 | a0001c0006t0001g0316 a0007c0019t0017g0314 a0007c0019t0017g0315 |
3 | HG03225.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.78+43546A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773966 | |||||||
| chr5:149773971 | A | G | 1 | a0002c0008t0008g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.78+43551A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149773971 | |||||||
| chr5:149774000 | G | A | 2 | a0003c0012t0014g0120 a0005c0011t0027g0132 |
2 | HG02723.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.78+43580G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149774000 | |||||||
| chr5:149774007 | G | A | 212 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0053 others(209): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.78+43587G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149774007 | |||||||
| chr5:149774021 | C | A | 1 | a0004c0005t0001g0121 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.78+43601C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149774021 | |||||||
| chr5:149774024 | C | T | 61 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0155 others(58): Show |
61 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.78+43604C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149774024 | |||||||
| chr5:149774086 | T | G | 1 | a0004c0005t0001g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.78+43666T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149774086 | |||||||
| chr5:149774160 | C | A | 1 | a0003c0012t0014g0120 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.78+43740C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149774160 | |||||||
| chr5:149774340 | C | T | 2 | a0001c0001t0003g0022 a0001c0001t0003g0024 |
2 | HG00099.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.78+43920C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149774340 | |||||||
| chr5:149774884 | C | G | 79 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(76): Show |
79 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.78+44464C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149774884 | |||||||
| chr5:149775160 | T | C | 83 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(80): Show |
83 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.78+44740T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775160 | |||||||
| chr5:149775221 | A | C | 1 | a0008c0016t0036g0122 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.78+44801A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775221 | |||||||
| chr5:149775272 | G | A | 231 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.78+44852G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775272 | |||||||
| chr5:149775282 | T | C | 1 | a0001c0001t0012g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.78+44862T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775282 | |||||||
| chr5:149775314 | C | T | 79 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(76): Show |
79 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.78+44894C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775314 | |||||||
| chr5:149775315 | G | A | 7 | a0003c0003t0004g0293 a0003c0003t0004g0294 a0003c0003t0004g0295 others(4): Show |
7 | HG01433.hp1 HG01496.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+44895G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775315 | |||||||
| chr5:149775342 | G | A | 4 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+44922G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775342 | |||||||
| chr5:149775476 | G | C | 8 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(5): Show |
8 | HG00140.hp1 HG00639.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-44957G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775476 | |||||||
| chr5:149775494 | C | T | 4 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-44939C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775494 | |||||||
| chr5:149775501 | C | T | 4 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-44932C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775501 | |||||||
| chr5:149775511 | G | A | 1 | a0002c0002t0066g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.79-44922G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775511 | |||||||
| chr5:149775545 | C | A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79-44888C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775545 | |||||||
| chr5:149775573 | C | T | 55 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(52): Show |
55 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.79-44860C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775573 | |||||||
| chr5:149775717 | A | AC | 231 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.79-44715dupC | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149775717 | ||||||
| chr5:149775766 | C | T | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-44667C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775766 | |||||||
| chr5:149775797 | G | T | 5 | a0001c0009t0064g0261 a0004c0005t0001g0121 a0005c0013t0001g0317 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-44636G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775797 | |||||||
| chr5:149775988 | TG | T | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-44444delG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149775988 | |||||||
| chr5:149776025 | C | G | 79 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(76): Show |
79 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-44408C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149776025 | |||||||
| chr5:149776138 | G | C | 4 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-44295G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149776138 | |||||||
| chr5:149776148 | TTCTAAC | T | 79 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(76): Show |
79 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-44279_79-44274d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149776148 | ||||||
| chr5:149776334 | A | C | 1 | a0001c0001t0001g0149 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.79-44099A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149776334 | |||||||
| chr5:149776341 | G | A | 2 | a0001c0030t0031g0320 a0002c0008t0008g0319 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.79-44092G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149776341 | |||||||
| chr5:149776373 | A | T | 5 | a0002c0002t0005g0006 a0002c0002t0005g0212 a0002c0002t0008g0003 others(2): Show |
5 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-44060A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149776373 | |||||||
| chr5:149776572 | G | A | 4 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-43861G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149776572 | |||||||
| chr5:149776604 | T | A | 5 | a0001c0009t0064g0261 a0004c0005t0001g0121 a0005c0013t0001g0317 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-43829T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149776604 | |||||||
| chr5:149776626 | G | A | 34 | a0001c0001t0003g0103 a0001c0001t0007g0106 a0001c0004t0006g0095 others(31): Show |
34 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.79-43807G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149776626 | |||||||
| chr5:149777177 | C | T | 79 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(76): Show |
79 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-43256C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777177 | |||||||
| chr5:149777178 | G | A | 4 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-43255G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777178 | |||||||
| chr5:149777199 | A | G | 5 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0083 others(2): Show |
5 | HG01952.hp1 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-43234A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777199 | |||||||
| chr5:149777258 | GACCCCTG others(3): Show |
G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-43171_79-43162d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777258 | ||||||
| chr5:149777406 | T | C | 3 | a0001c0006t0001g0316 a0007c0019t0017g0314 a0007c0019t0017g0315 |
3 | HG03225.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.79-43027T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777406 | |||||||
| chr5:149777448 | G | A | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-42985G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777448 | |||||||
| chr5:149777550 | C | T | 79 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(76): Show |
79 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-42883C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777550 | |||||||
| chr5:149777588 | A | G | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.79-42845A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777588 | |||||||
| chr5:149777751 | A | G | 230 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.79-42682A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777751 | |||||||
| chr5:149777784 | A | AAC | 21 | a0001c0001t0001g0226 a0001c0001t0001g0240 a0001c0001t0002g0268 others(18): Show |
21 | HG00099.hp1 HG00438.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79-42607_79-42606d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | AACAC | 24 | a0001c0001t0001g0002 a0001c0001t0019g0052 a0001c0001t0019g0082 others(21): Show |
24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.79-42609_79-42606d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | AACACAC | 41 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0070 others(38): Show |
41 | HG00438.hp1 HG00544.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.79-42611_79-42606d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | AACACACA others(1): Show |
33 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0062 others(30): Show |
33 | HG00280.hp2 HG00544.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.79-42613_79-42606d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | AACACACA others(3): Show |
6 | a0001c0001t0001g0047 a0001c0001t0001g0280 a0001c0001t0003g0087 others(3): Show |
6 | HG00609.hp1 HG02040.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-42615_79-42606d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | AACACACA others(5): Show |
3 | a0005c0013t0009g0008 a0006c0007t0016g0131 a0008c0016t0026g0262 |
3 | HG02922.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.79-42617_79-42606d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | AACACACA others(7): Show |
3 | a0001c0001t0007g0025 a0002c0002t0005g0084 a0005c0013t0009g0007 |
3 | HG03486.hp1 NA18994.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.79-42619_79-42606d others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | AACACACA others(9): Show |
1 | a0001c0001t0002g0068 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.79-42621_79-42606d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | AACACACA others(13): Show |
1 | a0002c0002t0010g0125 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.79-42625_79-42606d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.79-42649_79-42648i others(17): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777784 | |||||||
| chr5:149777784 | AAC | A | 34 | a0001c0001t0001g0201 a0001c0001t0001g0207 a0001c0001t0001g0220 others(31): Show |
34 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.79-42607_79-42606d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | AACAC | A | 65 | a0001c0001t0001g0143 a0001c0001t0001g0155 a0001c0001t0001g0161 others(62): Show |
65 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.79-42609_79-42606d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | AACACAC | A | 5 | a0001c0001t0001g0069 a0001c0001t0002g0134 a0001c0001t0002g0200 others(2): Show |
5 | HG02293.hp2 HG02523.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-42611_79-42606d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777784 | AACACACA others(9): Show |
A | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-42621_79-42606d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777784 | ||||||
| chr5:149777791 | A | ACACACAC others(63): Show |
1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79-42605_79-42604i others(72): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777791 | ||||||
| chr5:149777791 | A | ACACACAC others(61): Show |
1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-42608_79-42607i others(70): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777791 | ||||||
| chr5:149777800 | C | CACACACA others(209): Show |
1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79-42606_79-42605i others(218): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777800 | ||||||
| chr5:149777800 | C | CACACACA others(208): Show |
1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-42606_79-42605i others(217): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777800 | ||||||
| chr5:149777826 | C | G | 79 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(76): Show |
79 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-42607C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777826 | |||||||
| chr5:149777865 | T | TC | 16 | a0001c0001t0001g0067 a0001c0001t0001g0149 a0001c0001t0001g0271 others(13): Show |
16 | HG00408.hp1 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.79-42560dupC | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777865 | ||||||
| chr5:149777900 | G | A | 1 | a0017c0034t0013g0021 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.79-42533G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149777900 | |||||||
| chr5:149777922 | T | TCA | 60 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0205 others(57): Show |
60 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.79-42470_79-42469d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | T | TCACA | 11 | a0001c0001t0001g0228 a0001c0001t0002g0200 a0001c0001t0002g0268 others(8): Show |
11 | HG00140.hp1 HG02148.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-42472_79-42469d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | T | TCACACA | 11 | a0001c0001t0001g0010 a0001c0001t0001g0233 a0001c0001t0015g0289 others(8): Show |
11 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-42474_79-42469d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | T | TCACACAC others(1): Show |
7 | a0001c0006t0001g0316 a0005c0013t0001g0013 a0005c0013t0009g0007 others(4): Show |
7 | HG03195.hp2 HG03225.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-42476_79-42469d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | T | TCACACAC others(5): Show |
1 | a0008c0016t0026g0009 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79-42480_79-42469d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | T | TCACACAC others(9): Show |
1 | a0006c0007t0016g0012 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.79-42484_79-42469d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | TCA | T | 8 | a0001c0001t0002g0227 a0001c0001t0028g0214 a0001c0001t0045g0198 others(5): Show |
8 | HG02132.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-42470_79-42469d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | TCACA | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0312 a0001c0001t0047g0265 others(3): Show |
6 | HG02280.hp1 HG02896.hp2 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-42472_79-42469d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | TCACACA | T | 17 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0230 others(14): Show |
17 | HG01361.hp2 HG01433.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.79-42474_79-42469d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | TCACACAC others(1): Show |
T | 49 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0062 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.79-42476_79-42469d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | TCACACAC others(3): Show |
T | 22 | a0001c0001t0002g0134 a0001c0001t0003g0026 a0001c0001t0003g0172 others(19): Show |
22 | HG00408.hp2 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.79-42478_79-42469d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | TCACACAC others(5): Show |
T | 63 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.79-42480_79-42469d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | TCACACAC others(11): Show |
T | 1 | a0001c0004t0006g0105 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.79-42486_79-42469d others(20): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777922 | TCACACAC others(17): Show |
T | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.79-42492_79-42469d others(26): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777922 | ||||||
| chr5:149777928 | A | ACACACAC others(114): Show |
2 | a0002c0008t0008g0191 a0002c0008t0063g0169 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79-42479_79-42478i others(123): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777928 | ||||||
| chr5:149777935 | C | CACACACA others(3): Show |
1 | a0001c0017t0017g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.79-42489_79-42488i others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149777935 | ||||||
| chr5:149778003 | TC | T | 115 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(112): Show |
115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.79-42421delC | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778003 | ||||||
| chr5:149778012 | C | T | 109 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0053 others(106): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.79-42421C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778012 | |||||||
| chr5:149778060 | ATC | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0070 others(36): Show |
39 | HG00735.hp1 HG00741.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.79-42370_79-42369d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778060 | ||||||
| chr5:149778061 | T | TCA | 5 | a0001c0001t0001g0231 a0002c0002t0010g0038 a0002c0002t0065g0051 others(2): Show |
5 | HG01433.hp2 HG03041.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-42371_79-42370i others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | T | TCACA | 4 | a0001c0001t0001g0280 a0001c0001t0023g0229 a0002c0002t0005g0016 others(1): Show |
4 | HG00609.hp1 HG02559.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-42371_79-42370i others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCA | T | 68 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0062 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.79-42370_79-42367d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCACA | T | 44 | a0001c0001t0001g0053 a0001c0001t0001g0074 a0001c0001t0001g0228 others(41): Show |
44 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-42370_79-42365d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCACAC others(1): Show |
T | 25 | a0001c0001t0001g0155 a0001c0001t0002g0093 a0001c0001t0003g0022 others(22): Show |
25 | HG00099.hp2 HG01081.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.79-42370_79-42363d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCACAC others(3): Show |
T | 12 | a0001c0001t0003g0087 a0001c0001t0007g0106 a0001c0001t0020g0299 others(9): Show |
12 | HG01168.hp1 HG01496.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-42370_79-42361d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCACAC others(5): Show |
T | 34 | a0001c0001t0001g0165 a0001c0001t0002g0152 a0001c0001t0003g0103 others(31): Show |
34 | HG00280.hp2 HG00544.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.79-42370_79-42359d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCACAC others(7): Show |
T | 2 | a0002c0002t0008g0030 a0006c0007t0016g0131 |
2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.79-42370_79-42357d others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCACAC others(9): Show |
T | 4 | a0001c0001t0020g0126 a0001c0004t0006g0107 a0002c0002t0066g0079 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-42370_79-42355d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCACAC others(11): Show |
T | 4 | a0001c0017t0006g0078 a0001c0030t0031g0320 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-42370_79-42353d others(20): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778061 | TCTCACAC others(27): Show |
T | 5 | a0001c0009t0064g0261 a0004c0005t0001g0121 a0005c0013t0001g0317 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-42370_79-42337d others(36): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778061 | ||||||
| chr5:149778063 | T | A | 23 | a0001c0001t0001g0018 a0001c0001t0001g0092 a0001c0001t0001g0149 others(20): Show |
23 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.79-42370T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778063 | |||||||
| chr5:149778063 | T | TCA | 13 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0226 others(10): Show |
13 | HG00408.hp1 HG00438.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.79-42323_79-42322d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778063 | ||||||
| chr5:149778063 | T | TCACA | 9 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0002g0200 others(6): Show |
9 | HG00741.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-42325_79-42322d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778063 | ||||||
| chr5:149778063 | T | TCACACAC others(3): Show |
1 | a0001c0001t0053g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.79-42331_79-42322d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778063 | ||||||
| chr5:149778063 | TCA | T | 4 | a0001c0001t0001g0220 a0001c0001t0002g0194 a0001c0018t0029g0217 others(1): Show |
4 | HG00280.hp1 HG01074.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-42323_79-42322d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778063 | ||||||
| chr5:149778088 | CACACACA others(17): Show |
C | 7 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0057g0238 others(4): Show |
7 | HG01106.hp1 HG01346.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-42343_79-42320d others(26): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778088 | ||||||
| chr5:149778089 | A | G | 3 | a0001c0004t0006g0112 a0001c0004t0006g0115 a0001c0004t0030g0113 |
3 | HG00280.hp2 HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.79-42344A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778089 | |||||||
| chr5:149778092 | CACACACA others(13): Show |
C | 1 | a0001c0004t0030g0253 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79-42339_79-42320d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778092 | ||||||
| chr5:149778100 | CACACACA others(5): Show |
C | 3 | a0004c0005t0013g0241 a0004c0005t0022g0234 a0004c0005t0049g0243 |
3 | HG02165.hp2 HG03669.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.79-42331_79-42320d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778100 | ||||||
| chr5:149778108 | CACAG | C | 8 | a0001c0001t0001g0233 a0001c0001t0001g0258 a0001c0001t0047g0265 others(5): Show |
8 | HG01255.hp2 HG01934.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-42323_79-42320d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778108 | ||||||
| chr5:149778110 | CAG | C | 5 | a0001c0001t0015g0232 a0001c0010t0001g0255 a0001c0010t0001g0256 others(2): Show |
5 | HG00639.hp2 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-42320_79-42319d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778110 | ||||||
| chr5:149778112 | G | C | 259 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(256): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.79-42321G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778112 | |||||||
| chr5:149778122 | C | T | 4 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-42311C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778122 | |||||||
| chr5:149778145 | A | AAC | 89 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(86): Show |
89 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.79-42270_79-42269d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778145 | ||||||
| chr5:149778263 | A | G | 258 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(255): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.79-42170A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778263 | |||||||
| chr5:149778314 | C | T | 4 | a0001c0030t0031g0320 a0002c0008t0008g0319 a0013c0027t0037g0318 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-42119C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778314 | |||||||
| chr5:149778435 | C | T | 1 | a0001c0024t0001g0091 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.79-41998C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778435 | |||||||
| chr5:149778793 | A | G | 2 | a0001c0006t0001g0099 a0001c0006t0001g0100 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79-41640A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778793 | |||||||
| chr5:149778839 | AGT | A | 3 | a0002c0008t0008g0319 a0013c0027t0037g0318 a0014c0025t0031g0043 |
3 | HG02451.hp1 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.79-41587_79-41586d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149778839 | ||||||
| chr5:149778934 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79-41499C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149778934 | |||||||
| chr5:149779143 | A | G | 6 | a0001c0009t0064g0261 a0001c0030t0031g0320 a0004c0005t0001g0121 others(3): Show |
6 | HG02647.hp1 HG03041.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-41290A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779143 | |||||||
| chr5:149779241 | C | T | 1 | a0001c0001t0051g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.79-41192C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779241 | |||||||
| chr5:149779248 | A | G | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79-41185A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779248 | |||||||
| chr5:149779260 | T | A | 35 | a0001c0001t0003g0020 a0001c0001t0003g0103 a0001c0001t0007g0106 others(32): Show |
35 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.79-41173T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779260 | |||||||
| chr5:149779309 | C | G | 16 | a0001c0001t0001g0165 a0001c0001t0001g0312 a0001c0004t0018g0031 others(13): Show |
16 | HG02145.hp1 HG02280.hp1 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.79-41124C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779309 | |||||||
| chr5:149779500 | A | G | 3 | a0002c0008t0008g0319 a0013c0027t0037g0318 a0014c0025t0031g0043 |
3 | HG02451.hp1 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.79-40933A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779500 | |||||||
| chr5:149779504 | A | T | 6 | a0001c0009t0064g0261 a0001c0030t0031g0320 a0004c0005t0001g0121 others(3): Show |
6 | HG02647.hp1 HG03041.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-40929A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779504 | |||||||
| chr5:149779544 | A | G | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-40889A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779544 | |||||||
| chr5:149779611 | G | A | 73 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(70): Show |
73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.79-40822G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779611 | |||||||
| chr5:149779755 | A | C | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79-40678A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149779755 | |||||||
| chr5:149780219 | G | C | 5 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(2): Show |
5 | HG02723.hp1 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-40214G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780219 | |||||||
| chr5:149780238 | G | A | 2 | a0004c0015t0001g0119 a0004c0015t0001g0196 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.79-40195G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780238 | |||||||
| chr5:149780299 | C | G | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-40134C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780299 | |||||||
| chr5:149780422 | G | A | 195 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0143 others(192): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.79-40011G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780422 | |||||||
| chr5:149780489 | T | TG | 4 | a0001c0001t0002g0134 a0001c0001t0002g0152 a0001c0001t0002g0163 others(1): Show |
4 | HG01081.hp2 HG01261.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-39943dupG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149780489 | ||||||
| chr5:149780504 | A | G | 6 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-39929A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780504 | |||||||
| chr5:149780582 | G | C | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-39851G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780582 | |||||||
| chr5:149780599 | C | T | 6 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-39834C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780599 | |||||||
| chr5:149780616 | G | A | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.79-39817G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780616 | |||||||
| chr5:149780646 | T | A | 6 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-39787T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780646 | |||||||
| chr5:149780663 | A | G | 1 | a0002c0002t0068g0250 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79-39770A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780663 | |||||||
| chr5:149780746 | CAG | C | 3 | a0002c0008t0008g0319 a0013c0027t0037g0318 a0014c0025t0031g0043 |
3 | HG02451.hp1 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.79-39685_79-39684d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149780746 | ||||||
| chr5:149780859 | C | T | 1 | a0001c0001t0039g0141 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.79-39574C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780859 | |||||||
| chr5:149780860 | G | A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79-39573G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780860 | |||||||
| chr5:149780911 | A | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0006t0001g0316 others(10): Show |
13 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-39522A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780911 | |||||||
| chr5:149780931 | C | A | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-39502C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780931 | |||||||
| chr5:149780933 | G | C | 1 | a0001c0004t0030g0253 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79-39500G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149780933 | |||||||
| chr5:149781130 | G | A | 1 | a0004c0015t0001g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-39303G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149781130 | |||||||
| chr5:149781135 | G | A | 33 | a0001c0001t0001g0165 a0001c0001t0001g0312 a0001c0004t0018g0031 others(30): Show |
33 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(30): Show |
intron_variant | MODIFIER | c.79-39298G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149781135 | |||||||
| chr5:149781169 | C | T | 6 | a0001c0001t0015g0300 a0002c0002t0010g0304 a0002c0002t0025g0286 others(3): Show |
6 | HG00140.hp2 HG01943.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-39264C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149781169 | |||||||
| chr5:149781204 | C | CA | 125 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0143 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.79-39213dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149781204 | ||||||
| chr5:149781204 | CA | C | 21 | a0001c0001t0001g0098 a0001c0001t0002g0068 a0001c0001t0007g0025 others(18): Show |
21 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.79-39213delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149781204 | ||||||
| chr5:149781218 | A | G | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-39215A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149781218 | |||||||
| chr5:149781327 | G | A | 78 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(75): Show |
78 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.79-39106G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149781327 | |||||||
| chr5:149781781 | A | G | 6 | a0002c0002t0005g0006 a0002c0002t0005g0212 a0002c0002t0008g0003 others(3): Show |
6 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-38652A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149781781 | |||||||
| chr5:149781874 | C | T | 201 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0143 others(198): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.79-38559C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149781874 | |||||||
| chr5:149782298 | A | G | 1 | a0001c0001t0041g0222 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.79-38135A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782298 | |||||||
| chr5:149782398 | T | C | 1 | a0012c0031t0002g0235 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.79-38035T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782398 | |||||||
| chr5:149782519 | C | A | 77 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(74): Show |
77 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.79-37914C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782519 | |||||||
| chr5:149782655 | G | A | 5 | a0001c0009t0009g0130 a0002c0008t0005g0129 a0005c0011t0001g0128 others(2): Show |
5 | HG02723.hp1 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-37778G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782655 | |||||||
| chr5:149782683 | T | G | 170 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0143 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.79-37750T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782683 | |||||||
| chr5:149782731 | G | A | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-37702G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782731 | |||||||
| chr5:149782738 | G | A | 54 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(51): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.79-37695G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782738 | |||||||
| chr5:149782795 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.79-37638G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782795 | |||||||
| chr5:149782888 | G | A | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-37545G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782888 | |||||||
| chr5:149782976 | G | A | 22 | a0001c0001t0001g0165 a0001c0001t0001g0312 a0001c0004t0018g0031 others(19): Show |
22 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.79-37457G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149782976 | |||||||
| chr5:149783079 | G | A | 28 | a0001c0001t0001g0165 a0001c0001t0001g0312 a0001c0004t0018g0031 others(25): Show |
28 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.79-37354G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783079 | |||||||
| chr5:149783091 | A | AAGAG | 151 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(148): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.79-37326_79-37323d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149783091 | ||||||
| chr5:149783091 | A | AAGAGAG | 92 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0143 others(89): Show |
92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.79-37328_79-37323d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149783091 | ||||||
| chr5:149783091 | A | AAGAGAGA others(1): Show |
12 | a0001c0009t0064g0261 a0002c0002t0005g0006 a0002c0002t0005g0212 others(9): Show |
12 | HG02451.hp2 HG02647.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-37330_79-37323d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149783091 | ||||||
| chr5:149783215 | A | G | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79-37218A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783215 | |||||||
| chr5:149783471 | G | A | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-36962G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783471 | |||||||
| chr5:149783478 | A | G | 1 | a0001c0004t0006g0105 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.79-36955A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783478 | |||||||
| chr5:149783660 | G | A | 1 | a0002c0002t0010g0204 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.79-36773G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783660 | |||||||
| chr5:149783689 | C | T | 6 | a0002c0002t0005g0006 a0002c0002t0005g0212 a0002c0002t0008g0003 others(3): Show |
6 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-36744C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783689 | |||||||
| chr5:149783756 | T | G | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-36677T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783756 | |||||||
| chr5:149783851 | A | G | 255 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(252): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.79-36582A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783851 | |||||||
| chr5:149783891 | G | A | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-36542G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149783891 | |||||||
| chr5:149784237 | C | A | 1 | a0004c0005t0022g0109 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.79-36196C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784237 | |||||||
| chr5:149784278 | T | A | 8 | a0001c0009t0009g0130 a0001c0030t0031g0320 a0002c0002t0008g0030 others(5): Show |
8 | HG02723.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-36155T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784278 | |||||||
| chr5:149784325 | G | A | 35 | a0001c0001t0003g0020 a0001c0001t0003g0103 a0001c0001t0007g0106 others(32): Show |
35 | HG00280.hp2 HG00544.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.79-36108G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784325 | |||||||
| chr5:149784346 | G | A | 1 | a0004c0015t0001g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79-36087G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784346 | |||||||
| chr5:149784474 | C | G | 1 | a0001c0017t0006g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.79-35959C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784474 | |||||||
| chr5:149784529 | G | A | 1 | a0002c0002t0065g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79-35904G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784529 | |||||||
| chr5:149784560 | C | CT | 12 | a0001c0001t0002g0208 a0001c0001t0002g0268 a0001c0009t0009g0130 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.79-35850dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784560 | C | CTTTTTTT others(3): Show |
6 | a0002c0002t0005g0006 a0002c0002t0005g0212 a0002c0002t0008g0003 others(3): Show |
6 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-35866_79-35865i others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784560 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.79-35859_79-35850d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784560 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.79-35862_79-35850d others(15): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784560 | C | CTTTTTTT others(7): Show |
26 | a0001c0001t0001g0285 a0001c0001t0002g0275 a0001c0001t0002g0276 others(23): Show |
26 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.79-35863_79-35850d others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784560 | C | CTTTTTTT others(8): Show |
9 | a0002c0002t0010g0204 a0002c0002t0010g0304 a0003c0003t0004g0293 others(6): Show |
9 | HG01433.hp1 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-35864_79-35850d others(17): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784560 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0015g0289 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.79-35865_79-35850d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784560 | CT | C | 96 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(93): Show |
96 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.79-35850delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784560 | CTTTT | C | 102 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0053 others(99): Show |
102 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.79-35853_79-35850d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149784560 | ||||||
| chr5:149784604 | G | A | 258 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(255): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.79-35829G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784604 | |||||||
| chr5:149784606 | C | T | 93 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(90): Show |
93 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.79-35827C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784606 | |||||||
| chr5:149784672 | G | A | 258 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(255): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.79-35761G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784672 | |||||||
| chr5:149784692 | C | T | 53 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(50): Show |
53 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.79-35741C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784692 | |||||||
| chr5:149784710 | G | A | 4 | a0004c0015t0001g0118 a0004c0015t0001g0119 a0004c0015t0001g0196 others(1): Show |
4 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-35723G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784710 | |||||||
| chr5:149784724 | C | T | 253 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(250): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.79-35709C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784724 | |||||||
| chr5:149784802 | T | C | 257 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(254): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.79-35631T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784802 | |||||||
| chr5:149784803 | G | A | 37 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(34): Show |
37 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.79-35630G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784803 | |||||||
| chr5:149784814 | G | T | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-35619G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784814 | |||||||
| chr5:149784840 | T | G | 1 | a0001c0004t0006g0193 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.79-35593T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784840 | |||||||
| chr5:149784861 | C | T | 9 | a0001c0009t0009g0130 a0001c0010t0001g0056 a0001c0010t0001g0255 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-35572C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784861 | |||||||
| chr5:149784900 | G | A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79-35533G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784900 | |||||||
| chr5:149784901 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0006t0001g0316 others(10): Show |
13 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-35532T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149784901 | |||||||
| chr5:149785082 | T | C | 63 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(60): Show |
63 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.79-35351T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785082 | |||||||
| chr5:149785100 | G | A | 258 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(255): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.79-35333G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785100 | |||||||
| chr5:149785198 | A | T | 8 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(5): Show |
8 | HG00140.hp1 HG00639.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-35235A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785198 | |||||||
| chr5:149785260 | TG | T | 51 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(48): Show |
51 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.79-35170delG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149785260 | ||||||
| chr5:149785387 | A | G | 3 | a0001c0001t0015g0300 a0002c0002t0010g0304 a0003c0003t0004g0288 |
3 | HG02735.hp1 HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.79-35046A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785387 | |||||||
| chr5:149785464 | A | G | 1 | a0001c0010t0001g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.79-34969A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785464 | |||||||
| chr5:149785466 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79-34967G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785466 | |||||||
| chr5:149785607 | C | T | 1 | a0002c0002t0032g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79-34826C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785607 | |||||||
| chr5:149785709 | C | T | 1 | a0002c0002t0032g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79-34724C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785709 | |||||||
| chr5:149785734 | G | C | 9 | a0001c0009t0009g0130 a0001c0010t0001g0056 a0001c0010t0001g0255 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-34699G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785734 | |||||||
| chr5:149785781 | A | T | 1 | a0003c0003t0004g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.79-34652A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785781 | |||||||
| chr5:149785901 | C | G | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.79-34532C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785901 | |||||||
| chr5:149785915 | C | CT | 227 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.79-34502dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149785915 | ||||||
| chr5:149785915 | C | CTT | 7 | a0001c0001t0001g0186 a0001c0001t0002g0148 a0001c0001t0019g0052 others(4): Show |
7 | HG00099.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-34503_79-34502d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149785915 | ||||||
| chr5:149785934 | T | G | 77 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(74): Show |
77 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.79-34499T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149785934 | |||||||
| chr5:149786049 | A | C | 1 | a0001c0004t0006g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.79-34384A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786049 | |||||||
| chr5:149786116 | G | A | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-34317G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786116 | |||||||
| chr5:149786156 | G | A | 1 | a0001c0004t0018g0034 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79-34277G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786156 | |||||||
| chr5:149786159 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.79-34274C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786159 | |||||||
| chr5:149786305 | A | G | 9 | a0001c0001t0001g0143 a0001c0001t0001g0221 a0001c0001t0009g0142 others(6): Show |
9 | HG00735.hp1 HG00741.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-34128A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786305 | |||||||
| chr5:149786377 | T | C | 38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0274 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-34056T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786377 | |||||||
| chr5:149786489 | G | A | 77 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(74): Show |
77 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.79-33944G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786489 | |||||||
| chr5:149786598 | G | A | 3 | a0001c0001t0019g0052 a0001c0001t0019g0072 a0001c0001t0019g0082 |
3 | HG00099.hp1 HG01109.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.79-33835G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786598 | |||||||
| chr5:149786599 | C | T | 2 | a0001c0004t0006g0095 a0001c0033t0001g0096 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.79-33834C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786599 | |||||||
| chr5:149786666 | A | T | 182 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(179): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.79-33767A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786666 | |||||||
| chr5:149786692 | G | A | 1 | a0001c0004t0024g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79-33741G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786692 | |||||||
| chr5:149786750 | G | A | 3 | a0001c0006t0001g0316 a0007c0019t0017g0314 a0007c0019t0017g0315 |
3 | HG03225.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.79-33683G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786750 | |||||||
| chr5:149786871 | C | T | 182 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(179): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.79-33562C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149786871 | |||||||
| chr5:149787115 | G | A | 1 | a0002c0002t0005g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.79-33318G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149787115 | |||||||
| chr5:149787371 | C | A | 77 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(74): Show |
77 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.79-33062C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149787371 | |||||||
| chr5:149787435 | A | G | 2 | a0005c0011t0009g0054 a0005c0011t0009g0088 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.79-32998A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149787435 | |||||||
| chr5:149787510 | G | A | 12 | a0001c0001t0002g0148 a0001c0001t0007g0175 a0001c0001t0007g0176 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.79-32923G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149787510 | |||||||
| chr5:149787517 | A | G | 7 | a0002c0002t0005g0006 a0002c0002t0005g0028 a0002c0002t0005g0212 others(4): Show |
7 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-32916A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149787517 | |||||||
| chr5:149787629 | C | T | 182 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(179): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.79-32804C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149787629 | |||||||
| chr5:149787943 | T | G | 1 | a0001c0017t0006g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.79-32490T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149787943 | |||||||
| chr5:149787961 | G | C | 182 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(179): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.79-32472G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149787961 | |||||||
| chr5:149788187 | G | A | 1 | a0004c0005t0001g0171 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.79-32246G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788187 | |||||||
| chr5:149788495 | A | G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-31938A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788495 | |||||||
| chr5:149788499 | G | A | 1 | a0001c0001t0003g0174 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.79-31934G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788499 | |||||||
| chr5:149788638 | G | A | 1 | a0001c0004t0062g0252 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.79-31795G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788638 | |||||||
| chr5:149788659 | T | A | 233 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(230): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.79-31774T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788659 | |||||||
| chr5:149788678 | C | A | 4 | a0001c0030t0031g0320 a0004c0005t0001g0121 a0008c0016t0026g0262 others(1): Show |
4 | HG02647.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-31755C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788678 | |||||||
| chr5:149788754 | G | T | 2 | a0001c0010t0009g0036 a0006c0007t0016g0035 |
2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.79-31679G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788754 | |||||||
| chr5:149788817 | A | G | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.79-31616A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788817 | |||||||
| chr5:149788911 | C | A | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-31522C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149788911 | |||||||
| chr5:149789041 | C | T | 1 | a0001c0001t0021g0140 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.79-31392C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789041 | |||||||
| chr5:149789070 | C | T | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-31363C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789070 | |||||||
| chr5:149789149 | C | T | 49 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(46): Show |
49 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.79-31284C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789149 | |||||||
| chr5:149789191 | A | G | 1 | a0001c0017t0006g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.79-31242A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789191 | |||||||
| chr5:149789377 | G | A | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-31056G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789377 | |||||||
| chr5:149789473 | G | A | 79 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0228 others(76): Show |
79 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-30960G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789473 | |||||||
| chr5:149789673 | G | A | 4 | a0001c0001t0001g0312 a0002c0008t0008g0015 a0002c0008t0008g0191 others(1): Show |
4 | HG02145.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-30760G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789673 | |||||||
| chr5:149789873 | T | A | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.79-30560T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789873 | |||||||
| chr5:149789886 | G | A | 21 | a0001c0001t0001g0165 a0001c0004t0018g0031 a0001c0004t0018g0034 others(18): Show |
21 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.79-30547G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789886 | |||||||
| chr5:149789998 | G | A | 2 | a0008c0016t0026g0262 a0008c0016t0036g0122 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-30435G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149789998 | |||||||
| chr5:149790014 | C | T | 4 | a0001c0009t0064g0261 a0002c0002t0025g0027 a0002c0002t0025g0029 others(1): Show |
4 | HG00738.hp1 HG01993.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-30419C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149790014 | |||||||
| chr5:149790172 | C | G | 1 | a0001c0001t0021g0140 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.79-30261C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149790172 | |||||||
| chr5:149790365 | C | A | 8 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-30068C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149790365 | |||||||
| chr5:149790567 | A | T | 8 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-29866A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149790567 | |||||||
| chr5:149790723 | G | A | 1 | a0002c0008t0008g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.79-29710G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149790723 | |||||||
| chr5:149790757 | C | T | 181 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(178): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.79-29676C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149790757 | |||||||
| chr5:149791063 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.79-29370C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791063 | |||||||
| chr5:149791180 | G | C | 49 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(46): Show |
49 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.79-29253G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791180 | |||||||
| chr5:149791291 | C | CA | 9 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-29127dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149791291 | ||||||
| chr5:149791291 | CA | C | 172 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(169): Show |
172 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.79-29127delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149791291 | ||||||
| chr5:149791335 | G | C | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79-29098G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791335 | |||||||
| chr5:149791564 | AGT | A | 6 | a0001c0001t0002g0148 a0001c0001t0007g0175 a0001c0001t0007g0176 others(3): Show |
6 | NA18979.hp1 NA18980.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-28861_79-28860d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149791564 | ||||||
| chr5:149791577 | T | A | 182 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(179): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.79-28856T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791577 | |||||||
| chr5:149791662 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.79-28771G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791662 | |||||||
| chr5:149791687 | C | G | 1 | a0001c0001t0001g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.79-28746C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791687 | |||||||
| chr5:149791793 | C | T | 1 | a0002c0002t0005g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.79-28640C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791793 | |||||||
| chr5:149791803 | C | T | 7 | a0001c0001t0001g0240 a0001c0001t0057g0238 a0003c0003t0011g0237 others(4): Show |
7 | HG01106.hp1 HG01952.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-28630C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791803 | |||||||
| chr5:149791815 | T | A | 2 | a0001c0001t0003g0151 a0001c0001t0003g0170 |
2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.79-28618T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791815 | |||||||
| chr5:149791891 | A | G | 1 | a0001c0001t0019g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.79-28542A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149791891 | |||||||
| chr5:149792028 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.79-28405G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792028 | |||||||
| chr5:149792246 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0017t0017g0014 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-28187C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792246 | |||||||
| chr5:149792326 | C | G | 30 | a0001c0001t0001g0233 a0001c0001t0001g0240 a0001c0001t0001g0258 others(27): Show |
30 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.79-28107C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792326 | |||||||
| chr5:149792594 | T | G | 1 | a0001c0001t0002g0227 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.79-27839T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792594 | |||||||
| chr5:149792595 | C | G | 1 | a0001c0001t0001g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.79-27838C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792595 | |||||||
| chr5:149792602 | A | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0201 a0001c0001t0001g0206 others(62): Show |
65 | HG00280.hp2 HG00438.hp2 HG01168.hp1 others(62): Show |
intron_variant | MODIFIER | c.79-27831A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792602 | |||||||
| chr5:149792604 | C | G | 8 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(5): Show |
8 | HG00140.hp1 HG00639.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-27829C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792604 | |||||||
| chr5:149792607 | T | C | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.79-27826T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792607 | |||||||
| chr5:149792694 | G | A | 51 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(48): Show |
51 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.79-27739G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792694 | |||||||
| chr5:149792727 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.79-27706T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792727 | |||||||
| chr5:149792735 | T | A | 1 | a0003c0003t0004g0287 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.79-27698T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792735 | |||||||
| chr5:149792738 | TATTC | T | 17 | a0001c0001t0001g0312 a0001c0001t0015g0300 a0001c0009t0064g0261 others(14): Show |
17 | HG00140.hp2 HG01943.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.79-27665_79-27662d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149792738 | ||||||
| chr5:149792760 | T | G | 246 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.79-27673T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792760 | |||||||
| chr5:149792768 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0002g0278 a0001c0004t0006g0277 |
3 | HG00738.hp2 HG02109.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.79-27665T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149792768 | |||||||
| chr5:149793008 | A | C | 1 | a0002c0008t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79-27425A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149793008 | |||||||
| chr5:149793408 | C | T | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.79-27025C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149793408 | |||||||
| chr5:149793415 | C | T | 3 | a0001c0030t0031g0320 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.79-27018C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149793415 | |||||||
| chr5:149793455 | C | T | 1 | a0001c0004t0006g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.79-26978C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149793455 | |||||||
| chr5:149793571 | A | G | 215 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0143 others(212): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.79-26862A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149793571 | |||||||
| chr5:149793719 | G | A | 119 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.79-26714G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149793719 | |||||||
| chr5:149793783 | C | T | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.79-26650C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149793783 | |||||||
| chr5:149794023 | C | T | 96 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(93): Show |
96 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.79-26410C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794023 | |||||||
| chr5:149794287 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79-26146C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794287 | |||||||
| chr5:149794309 | A | G | 3 | a0002c0008t0008g0191 a0002c0008t0008g0319 a0002c0008t0063g0169 |
3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.79-26124A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794309 | |||||||
| chr5:149794388 | G | A | 2 | a0001c0009t0064g0261 a0005c0013t0001g0317 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.79-26045G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794388 | |||||||
| chr5:149794438 | ACT | A | 54 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(51): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.79-25991_79-25990d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794438 | ||||||
| chr5:149794507 | C | T | 2 | a0002c0008t0008g0191 a0002c0008t0063g0169 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79-25926C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794507 | |||||||
| chr5:149794514 | A | G | 54 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(51): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.79-25919A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794514 | |||||||
| chr5:149794524 | G | GCA | 4 | a0001c0009t0064g0261 a0002c0002t0010g0264 a0005c0013t0001g0317 others(1): Show |
4 | HG02965.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-25880_79-25879d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794524 | G | GCACA | 11 | a0001c0001t0001g0165 a0001c0001t0012g0048 a0001c0001t0048g0049 others(8): Show |
11 | HG02280.hp1 HG02630.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-25882_79-25879d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794524 | G | GCACACA | 14 | a0001c0001t0001g0053 a0001c0001t0001g0230 a0001c0001t0001g0231 others(11): Show |
14 | HG01361.hp2 HG01433.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-25884_79-25879d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794524 | G | GCACACAC others(1): Show |
38 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0069 others(35): Show |
38 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-25886_79-25879d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794524 | G | GCACACAC others(3): Show |
7 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0074 others(4): Show |
7 | HG01952.hp1 HG01975.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-25888_79-25879d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794524 | GCA | G | 4 | a0001c0006t0001g0316 a0002c0008t0008g0015 a0007c0019t0017g0314 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-25880_79-25879d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794524 | GCACA | G | 93 | a0001c0001t0001g0010 a0001c0001t0001g0201 a0001c0001t0001g0220 others(90): Show |
93 | HG00280.hp2 HG00639.hp2 HG01069.hp1 others(90): Show |
intron_variant | MODIFIER | c.79-25882_79-25879d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794524 | GCACACA | G | 6 | a0001c0001t0003g0022 a0002c0002t0008g0030 a0002c0002t0008g0055 others(3): Show |
6 | HG00099.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-25884_79-25879d others(8): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794524 | GCACACAC others(1): Show |
G | 37 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(34): Show |
37 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.79-25886_79-25879d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149794524 | ||||||
| chr5:149794551 | CACAT | C | 66 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0155 others(63): Show |
66 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.79-25881_79-25878d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794551 | |||||||
| chr5:149794553 | CAT | C | 5 | a0001c0001t0001g0018 a0001c0001t0003g0182 a0002c0002t0005g0179 others(2): Show |
5 | HG02056.hp1 HG02135.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-25879_79-25878d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794553 | |||||||
| chr5:149794822 | C | T | 1 | a0003c0012t0014g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.79-25611C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794822 | |||||||
| chr5:149794902 | C | T | 2 | a0001c0001t0045g0198 a0001c0018t0029g0197 |
2 | HG01175.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79-25531C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794902 | |||||||
| chr5:149794903 | A | G | 214 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0053 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.79-25530A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794903 | |||||||
| chr5:149794977 | G | A | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-25456G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149794977 | |||||||
| chr5:149795005 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0020g0126 |
3 | NA18945.hp1 NA18990.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.79-25428G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795005 | |||||||
| chr5:149795103 | C | G | 1 | a0006c0007t0060g0032 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79-25330C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795103 | |||||||
| chr5:149795257 | A | G | 2 | a0001c0001t0045g0198 a0001c0018t0029g0197 |
2 | HG01175.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.79-25176A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795257 | |||||||
| chr5:149795271 | C | A | 8 | a0002c0002t0005g0006 a0002c0002t0005g0028 a0002c0002t0005g0212 others(5): Show |
8 | HG00735.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-25162C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795271 | |||||||
| chr5:149795389 | G | A | 43 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(40): Show |
43 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.79-25044G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795389 | |||||||
| chr5:149795455 | C | T | 7 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-24978C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795455 | |||||||
| chr5:149795649 | G | A | 1 | a0001c0018t0029g0197 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.79-24784G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795649 | |||||||
| chr5:149795664 | C | A | 7 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-24769C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795664 | |||||||
| chr5:149795787 | G | T | 1 | a0001c0001t0002g0307 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.79-24646G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795787 | |||||||
| chr5:149795789 | AG | A | 71 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(68): Show |
71 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.79-24637delG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149795789 | ||||||
| chr5:149795791 | G | C | 5 | a0001c0001t0007g0106 a0001c0004t0006g0101 a0001c0004t0006g0104 others(2): Show |
5 | NA18974.hp1 NA18999.hp1 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-24642G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795791 | |||||||
| chr5:149795814 | T | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0165 others(76): Show |
79 | HG00280.hp2 HG00438.hp2 HG01168.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-24619T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795814 | |||||||
| chr5:149795814 | T | TC | 14 | a0001c0001t0001g0312 a0001c0009t0064g0261 a0001c0010t0001g0056 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.79-24618dupC | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149795814 | ||||||
| chr5:149795875 | G | A | 4 | a0001c0001t0001g0312 a0001c0009t0064g0261 a0001c0030t0031g0320 others(1): Show |
4 | HG03041.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-24558G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149795875 | |||||||
| chr5:149796101 | T | C | 296 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.79-24332T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796101 | |||||||
| chr5:149796180 | G | C | 6 | a0002c0002t0005g0006 a0002c0002t0005g0028 a0002c0002t0005g0212 others(3): Show |
6 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-24253G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796180 | |||||||
| chr5:149796222 | G | A | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-24211G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796222 | |||||||
| chr5:149796243 | T | G | 32 | a0001c0001t0001g0233 a0001c0001t0001g0240 a0001c0001t0001g0312 others(29): Show |
32 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.79-24190T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796243 | |||||||
| chr5:149796361 | A | G | 17 | a0001c0009t0064g0261 a0001c0010t0001g0056 a0001c0010t0001g0255 others(14): Show |
17 | HG00735.hp2 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.79-24072A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796361 | |||||||
| chr5:149796398 | G | A | 1 | a0003c0012t0014g0110 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.79-24035G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796398 | |||||||
| chr5:149796655 | A | G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-23778A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796655 | |||||||
| chr5:149796693 | A | G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-23740A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796693 | |||||||
| chr5:149796834 | C | A | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.79-23599C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796834 | |||||||
| chr5:149796920 | A | G | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-23513A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796920 | |||||||
| chr5:149796954 | C | G | 6 | a0001c0001t0001g0149 a0001c0001t0001g0242 a0001c0009t0009g0130 others(3): Show |
6 | HG01243.hp1 HG01346.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-23479C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149796954 | |||||||
| chr5:149797017 | C | T | 2 | a0001c0010t0056g0153 a0001c0017t0006g0078 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.79-23416C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797017 | |||||||
| chr5:149797126 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.79-23307C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797126 | |||||||
| chr5:149797141 | A | G | 8 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(5): Show |
8 | HG00735.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-23292A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797141 | |||||||
| chr5:149797276 | G | A | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-23157G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797276 | |||||||
| chr5:149797382 | T | C | 72 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0149 others(69): Show |
72 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.79-23051T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797382 | |||||||
| chr5:149797441 | A | G | 8 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(5): Show |
8 | HG00735.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-22992A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797441 | |||||||
| chr5:149797676 | C | A | 4 | a0001c0006t0001g0199 a0001c0006t0001g0209 a0001c0006t0001g0313 others(1): Show |
4 | HG01496.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-22757C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797676 | |||||||
| chr5:149797791 | T | C | 7 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-22642T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797791 | |||||||
| chr5:149797964 | A | G | 59 | a0001c0001t0001g0201 a0001c0001t0001g0220 a0001c0001t0001g0228 others(56): Show |
59 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.79-22469A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149797964 | |||||||
| chr5:149798066 | A | G | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-22367A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798066 | |||||||
| chr5:149798113 | T | A | 1 | a0001c0001t0003g0172 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.79-22320T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798113 | |||||||
| chr5:149798113 | T | C | 1 | a0002c0002t0010g0125 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.79-22320T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798113 | |||||||
| chr5:149798209 | C | T | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-22224C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798209 | |||||||
| chr5:149798251 | A | G | 2 | a0001c0001t0003g0057 a0001c0001t0003g0182 |
2 | NA18948.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.79-22182A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798251 | |||||||
| chr5:149798359 | T | A | 58 | a0001c0001t0001g0201 a0001c0001t0001g0220 a0001c0001t0001g0228 others(55): Show |
58 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.79-22074T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798359 | |||||||
| chr5:149798386 | C | T | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-22047C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798386 | |||||||
| chr5:149798610 | C | A | 60 | a0001c0001t0001g0201 a0001c0001t0001g0220 a0001c0001t0001g0228 others(57): Show |
60 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(57): Show |
intron_variant | MODIFIER | c.79-21823C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798610 | |||||||
| chr5:149798638 | A | G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-21795A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798638 | |||||||
| chr5:149798864 | T | G | 1 | a0001c0004t0006g0277 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.79-21569T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798864 | |||||||
| chr5:149798867 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79-21566G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798867 | |||||||
| chr5:149798916 | T | C | 1 | a0012c0031t0002g0235 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.79-21517T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798916 | |||||||
| chr5:149798978 | C | T | 11 | a0001c0001t0001g0165 a0001c0004t0018g0031 a0001c0004t0018g0034 others(8): Show |
11 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-21455C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798978 | |||||||
| chr5:149798980 | T | A | 15 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(12): Show |
15 | HG00735.hp2 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.79-21453T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149798980 | |||||||
| chr5:149799056 | C | CT | 80 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(77): Show |
80 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.79-21376dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799056 | ||||||
| chr5:149799158 | C | A | 1 | a0004c0005t0001g0139 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.79-21275C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799158 | |||||||
| chr5:149799433 | T | C | 23 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.79-21000T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799433 | |||||||
| chr5:149799459 | T | C | 290 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.79-20974T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799459 | |||||||
| chr5:149799621 | G | T | 1 | a0017c0034t0013g0021 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.79-20812G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799621 | |||||||
| chr5:149799661 | G | A | 1 | a0005c0013t0009g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79-20772G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799661 | |||||||
| chr5:149799687 | G | GTTTTTTT others(8): Show |
1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-20744_79-20743i others(17): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799687 | ||||||
| chr5:149799687 | G | GTTTTTTT others(16): Show |
1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-20744_79-20743i others(25): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799687 | ||||||
| chr5:149799690 | G | GTTT | 3 | a0001c0001t0012g0046 a0001c0024t0001g0091 a0002c0002t0010g0125 |
3 | NA18963.hp1 NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.79-20741_79-20740i others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799690 | ||||||
| chr5:149799690 | G | GTTTT | 53 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(50): Show |
53 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.79-20741_79-20740i others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799690 | ||||||
| chr5:149799690 | G | GTTTTT | 12 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0230 others(9): Show |
12 | HG01109.hp2 HG01361.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.79-20741_79-20740i others(7): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799690 | ||||||
| chr5:149799690 | G | GTTTTTTT others(5): Show |
2 | a0001c0018t0029g0217 a0001c0018t0058g0211 |
2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.79-20741_79-20740i others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799690 | ||||||
| chr5:149799690 | G | GTTTTTTT others(6): Show |
1 | a0001c0018t0029g0197 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.79-20741_79-20740i others(15): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799690 | ||||||
| chr5:149799690 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79-20741_79-20740i others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799690 | ||||||
| chr5:149799690 | G | T | 2 | a0002c0002t0008g0030 a0005c0013t0001g0317 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.79-20743G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799690 | |||||||
| chr5:149799690 | GTTGTT | G | 7 | a0002c0002t0005g0006 a0002c0002t0005g0028 a0002c0002t0005g0212 others(4): Show |
7 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-20740_79-20736d others(7): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799690 | ||||||
| chr5:149799693 | G | GT | 54 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0143 others(51): Show |
54 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.79-20719dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | GTT | 17 | a0001c0001t0001g0018 a0001c0001t0001g0149 a0001c0001t0001g0221 others(14): Show |
17 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.79-20720_79-20719d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | GTTGTTGT others(19): Show |
1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.79-20738_79-20737i others(28): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | GTTGTTTT | 8 | a0001c0001t0001g0165 a0001c0004t0018g0031 a0001c0004t0018g0034 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-20738_79-20737i others(9): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | GTTTTTTT others(1): Show |
38 | a0001c0001t0001g0271 a0001c0001t0001g0285 a0001c0001t0002g0148 others(35): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-20726_79-20719d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | GTTTTTTT others(2): Show |
41 | a0001c0001t0001g0220 a0001c0001t0001g0240 a0001c0001t0001g0312 others(38): Show |
41 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.79-20727_79-20719d others(11): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | GTTTTTTT others(3): Show |
20 | a0001c0001t0003g0024 a0001c0001t0003g0058 a0001c0004t0006g0095 others(17): Show |
20 | HG00639.hp2 HG01081.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.79-20728_79-20719d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | GTTTTTTT others(4): Show |
4 | a0001c0001t0057g0238 a0002c0002t0068g0250 a0004c0005t0001g0246 others(1): Show |
4 | HG01106.hp1 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-20729_79-20719d others(13): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | GTTTTTTT others(5): Show |
1 | a0004c0005t0001g0248 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.79-20730_79-20719d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799693 | G | T | 76 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.79-20740G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799693 | |||||||
| chr5:149799693 | GT | G | 8 | a0001c0001t0002g0173 a0001c0010t0009g0036 a0002c0002t0008g0055 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-20719delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149799693 | ||||||
| chr5:149799784 | G | A | 57 | a0001c0001t0001g0201 a0001c0001t0001g0220 a0001c0001t0001g0228 others(54): Show |
57 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(54): Show |
intron_variant | MODIFIER | c.79-20649G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799784 | |||||||
| chr5:149799790 | C | T | 107 | a0001c0001t0001g0165 a0001c0001t0001g0201 a0001c0001t0001g0220 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.79-20643C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799790 | |||||||
| chr5:149799839 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79-20594A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799839 | |||||||
| chr5:149799843 | G | A | 1 | a0002c0008t0008g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.79-20590G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149799843 | |||||||
| chr5:149800025 | C | A | 1 | a0004c0005t0001g0257 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.79-20408C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800025 | |||||||
| chr5:149800063 | AAAG | A | 31 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-20366_79-20364d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149800063 | ||||||
| chr5:149800141 | A | G | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-20292A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800141 | |||||||
| chr5:149800162 | T | C | 18 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(15): Show |
18 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.79-20271T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800162 | |||||||
| chr5:149800178 | C | A | 31 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-20255C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800178 | |||||||
| chr5:149800329 | C | T | 2 | a0001c0006t0001g0099 a0001c0006t0001g0100 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79-20104C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800329 | |||||||
| chr5:149800331 | A | C | 17 | a0001c0001t0001g0165 a0001c0004t0018g0031 a0001c0004t0018g0034 others(14): Show |
17 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.79-20102A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800331 | |||||||
| chr5:149800398 | C | T | 31 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-20035C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800398 | |||||||
| chr5:149800403 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.79-20030C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800403 | |||||||
| chr5:149800420 | T | C | 31 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-20013T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800420 | |||||||
| chr5:149800520 | G | A | 2 | a0001c0001t0015g0300 a0002c0002t0010g0304 |
2 | HG02735.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.79-19913G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800520 | |||||||
| chr5:149800970 | C | T | 12 | a0001c0001t0001g0062 a0001c0001t0001g0083 a0001c0001t0012g0046 others(9): Show |
12 | HG01952.hp1 HG01975.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.79-19463C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149800970 | |||||||
| chr5:149801270 | C | T | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.79-19163C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149801270 | |||||||
| chr5:149801311 | G | A | 3 | a0001c0001t0019g0052 a0001c0001t0019g0072 a0001c0001t0019g0082 |
3 | HG00099.hp1 HG01109.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.79-19122G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149801311 | |||||||
| chr5:149801431 | G | A | 57 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(54): Show |
57 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.79-19002G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149801431 | |||||||
| chr5:149801634 | AGGGAGCC others(3): Show |
A | 3 | a0004c0005t0001g0139 a0004c0005t0001g0245 a0004c0005t0012g0249 |
3 | HG01106.hp2 HG01258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.79-18795_79-18786d others(12): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149801634 | ||||||
| chr5:149801803 | C | T | 150 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.79-18630C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149801803 | |||||||
| chr5:149801823 | G | A | 31 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-18610G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149801823 | |||||||
| chr5:149801949 | G | A | 1 | a0002c0014t0005g0259 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.79-18484G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149801949 | |||||||
| chr5:149801959 | A | G | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-18474A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149801959 | |||||||
| chr5:149802715 | G | A | 2 | a0002c0008t0008g0191 a0002c0008t0063g0169 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79-17718G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149802715 | |||||||
| chr5:149802722 | C | T | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-17711C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149802722 | |||||||
| chr5:149802749 | C | T | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79-17684C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149802749 | |||||||
| chr5:149802760 | T | G | 2 | a0002c0008t0008g0191 a0002c0008t0063g0169 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79-17673T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149802760 | |||||||
| chr5:149802884 | G | T | 79 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(76): Show |
79 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-17549G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149802884 | |||||||
| chr5:149803056 | C | T | 1 | a0001c0001t0019g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.79-17377C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803056 | |||||||
| chr5:149803133 | C | T | 57 | a0001c0001t0001g0201 a0001c0001t0001g0220 a0001c0001t0001g0228 others(54): Show |
57 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(54): Show |
intron_variant | MODIFIER | c.79-17300C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803133 | |||||||
| chr5:149803269 | G | C | 31 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-17164G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803269 | |||||||
| chr5:149803294 | G | A | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-17139G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803294 | |||||||
| chr5:149803336 | C | G | 1 | a0001c0033t0001g0096 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.79-17097C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803336 | |||||||
| chr5:149803587 | G | C | 2 | a0002c0002t0005g0016 a0003c0003t0052g0192 |
2 | NA19012.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.79-16846G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803587 | |||||||
| chr5:149803693 | G | T | 19 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(16): Show |
19 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.79-16740G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803693 | |||||||
| chr5:149803797 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0149 others(1): Show |
4 | HG01346.hp1 HG01978.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-16636A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803797 | |||||||
| chr5:149803806 | G | T | 8 | a0001c0001t0001g0165 a0001c0004t0018g0031 a0001c0004t0018g0034 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-16627G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803806 | |||||||
| chr5:149803813 | G | A | 1 | a0001c0004t0006g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79-16620G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803813 | |||||||
| chr5:149803813 | G | T | 79 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(76): Show |
79 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-16620G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803813 | |||||||
| chr5:149803822 | C | T | 4 | a0001c0001t0003g0026 a0001c0001t0003g0103 a0001c0001t0003g0158 others(1): Show |
4 | HG00544.hp2 HG02083.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-16611C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149803822 | |||||||
| chr5:149804123 | C | T | 1 | a0003c0003t0011g0302 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.79-16310C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804123 | |||||||
| chr5:149804163 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0149 others(5): Show |
8 | HG00558.hp1 HG01346.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-16270C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804163 | |||||||
| chr5:149804165 | A | G | 6 | a0002c0002t0005g0006 a0002c0002t0005g0212 a0002c0002t0008g0003 others(3): Show |
6 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-16268A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804165 | |||||||
| chr5:149804233 | C | A | 2 | a0008c0016t0026g0262 a0008c0016t0036g0122 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-16200C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804233 | |||||||
| chr5:149804252 | G | A | 15 | a0001c0001t0001g0165 a0001c0004t0018g0031 a0001c0004t0018g0034 others(12): Show |
15 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.79-16181G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804252 | |||||||
| chr5:149804290 | TG | T | 58 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(55): Show |
58 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.79-16140delG | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149804290 | ||||||
| chr5:149804401 | C | T | 2 | a0001c0001t0001g0220 a0001c0017t0006g0219 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.79-16032C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804401 | |||||||
| chr5:149804495 | G | A | 2 | a0002c0008t0005g0129 a0005c0011t0001g0128 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.79-15938G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804495 | |||||||
| chr5:149804652 | A | G | 1 | a0001c0004t0006g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.79-15781A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804652 | |||||||
| chr5:149804862 | G | A | 1 | a0002c0002t0005g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.79-15571G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804862 | |||||||
| chr5:149804893 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.79-15540G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804893 | |||||||
| chr5:149804936 | C | T | 14 | a0001c0009t0064g0261 a0001c0018t0029g0197 a0001c0018t0029g0217 others(11): Show |
14 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.79-15497C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149804936 | |||||||
| chr5:149805099 | C | T | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-15334C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149805099 | |||||||
| chr5:149805186 | G | A | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-15247G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149805186 | |||||||
| chr5:149805342 | G | T | 32 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(29): Show |
32 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.79-15091G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149805342 | |||||||
| chr5:149805584 | C | T | 1 | a0005c0013t0009g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79-14849C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149805584 | |||||||
| chr5:149805659 | C | T | 2 | a0001c0010t0038g0185 a0002c0008t0071g0184 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.79-14774C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149805659 | |||||||
| chr5:149805726 | C | G | 272 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(269): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.79-14707C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149805726 | |||||||
| chr5:149805807 | A | G | 4 | a0002c0002t0008g0003 a0002c0002t0008g0055 a0005c0011t0009g0054 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-14626A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149805807 | |||||||
| chr5:149806140 | T | A | 1 | a0004c0005t0055g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.79-14293T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806140 | |||||||
| chr5:149806206 | C | T | 5 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 others(2): Show |
5 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-14227C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806206 | |||||||
| chr5:149806207 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.79-14226G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806207 | |||||||
| chr5:149806219 | G | A | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-14214G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806219 | |||||||
| chr5:149806360 | C | A | 19 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(16): Show |
19 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.79-14073C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806360 | |||||||
| chr5:149806401 | C | G | 2 | a0002c0002t0025g0027 a0002c0002t0025g0029 |
2 | HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.79-14032C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806401 | |||||||
| chr5:149806514 | G | A | 286 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.79-13919G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806514 | |||||||
| chr5:149806533 | G | A | 1 | a0003c0003t0004g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.79-13900G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806533 | |||||||
| chr5:149806608 | CTTTTTTT | C | 285 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(282): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.79-13813_79-13807d others(9): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149806608 | ||||||
| chr5:149806633 | G | GT | 81 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(78): Show |
81 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.79-13797dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149806633 | ||||||
| chr5:149806647 | G | A | 81 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(78): Show |
81 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.79-13786G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806647 | |||||||
| chr5:149806710 | C | T | 80 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(77): Show |
80 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.79-13723C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806710 | |||||||
| chr5:149806813 | G | A | 1 | a0003c0003t0004g0294 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79-13620G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806813 | |||||||
| chr5:149806858 | T | C | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-13575T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806858 | |||||||
| chr5:149806914 | TA | T | 21 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(18): Show |
21 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.79-13511delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149806914 | ||||||
| chr5:149806915 | A | T | 31 | a0001c0001t0001g0285 a0001c0001t0002g0274 a0001c0001t0002g0275 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-13518A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149806915 | |||||||
| chr5:149806956 | C | CT | 6 | a0001c0001t0002g0307 a0001c0001t0003g0135 a0001c0009t0064g0261 others(3): Show |
6 | HG01074.hp2 HG02738.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-13466dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149806956 | ||||||
| chr5:149807026 | C | G | 1 | a0001c0004t0030g0253 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79-13407C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807026 | |||||||
| chr5:149807056 | A | G | 158 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0061 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.79-13377A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807056 | |||||||
| chr5:149807383 | T | C | 1 | a0008c0016t0026g0009 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79-13050T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807383 | |||||||
| chr5:149807475 | A | G | 292 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.79-12958A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807475 | |||||||
| chr5:149807491 | G | A | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-12942G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807491 | |||||||
| chr5:149807571 | G | A | 80 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(77): Show |
80 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.79-12862G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807571 | |||||||
| chr5:149807611 | G | T | 81 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(78): Show |
81 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.79-12822G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807611 | |||||||
| chr5:149807649 | C | T | 21 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(18): Show |
21 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.79-12784C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807649 | |||||||
| chr5:149807759 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0240 a0001c0001t0003g0022 others(56): Show |
59 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.79-12674G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807759 | |||||||
| chr5:149807830 | C | T | 81 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0074 others(78): Show |
81 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.79-12603C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807830 | |||||||
| chr5:149807894 | C | T | 55 | a0001c0001t0001g0201 a0001c0001t0001g0220 a0001c0001t0001g0228 others(52): Show |
55 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.79-12539C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149807894 | |||||||
| chr5:149808077 | G | A | 21 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(18): Show |
21 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.79-12356G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808077 | |||||||
| chr5:149808087 | G | A | 1 | a0001c0001t0020g0137 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.79-12346G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808087 | |||||||
| chr5:149808219 | C | G | 2 | a0004c0015t0001g0119 a0004c0015t0001g0196 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.79-12214C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808219 | |||||||
| chr5:149808365 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0149 others(5): Show |
8 | HG00558.hp1 HG01346.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-12068C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808365 | |||||||
| chr5:149808565 | T | A | 291 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.79-11868T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808565 | |||||||
| chr5:149808566 | G | C | 58 | a0001c0001t0001g0201 a0001c0001t0001g0220 a0001c0001t0001g0228 others(55): Show |
58 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.79-11867G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808566 | |||||||
| chr5:149808707 | C | T | 1 | a0002c0002t0025g0029 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.79-11726C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808707 | |||||||
| chr5:149808749 | C | T | 2 | a0001c0001t0003g0123 a0003c0012t0014g0157 |
2 | HG02523.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.79-11684C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808749 | |||||||
| chr5:149808770 | C | T | 1 | a0002c0008t0071g0184 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.79-11663C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808770 | |||||||
| chr5:149808913 | A | G | 1 | a0001c0001t0040g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.79-11520A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149808913 | |||||||
| chr5:149809115 | T | A | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-11318T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809115 | |||||||
| chr5:149809115 | T | C | 1 | a0001c0001t0002g0282 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.79-11318T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809115 | |||||||
| chr5:149809115 | T | TTAGA | 80 | a0001c0001t0001g0010 a0001c0001t0001g0076 a0001c0001t0001g0094 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.79-11272_79-11269d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809115 | ||||||
| chr5:149809115 | T | TTAGATAG others(1): Show |
23 | a0001c0001t0001g0047 a0001c0001t0001g0226 a0001c0001t0001g0312 others(20): Show |
23 | HG00438.hp2 HG00639.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.79-11276_79-11269d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809115 | ||||||
| chr5:149809115 | T | TTAGATAG others(5): Show |
4 | a0001c0001t0001g0098 a0001c0001t0002g0200 a0001c0001t0002g0227 others(1): Show |
4 | HG02132.hp1 HG03225.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11280_79-11269d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809115 | ||||||
| chr5:149809115 | T | TTAGATAG others(9): Show |
1 | a0012c0031t0002g0235 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.79-11284_79-11269d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809115 | ||||||
| chr5:149809115 | TTAGA | T | 27 | a0001c0001t0001g0061 a0001c0001t0001g0233 a0001c0001t0002g0307 others(24): Show |
27 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.79-11272_79-11269d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809115 | ||||||
| chr5:149809115 | TTAGATAG others(1): Show |
T | 4 | a0001c0001t0001g0092 a0002c0002t0008g0003 a0004c0015t0001g0119 others(1): Show |
4 | HG00544.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11276_79-11269d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809115 | ||||||
| chr5:149809115 | TTAGATAG others(5): Show |
T | 2 | a0005c0011t0009g0054 a0005c0011t0009g0088 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.79-11280_79-11269d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809115 | ||||||
| chr5:149809115 | TTAGATAG others(115): Show |
T | 1 | a0002c0002t0008g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.79-11276_79-11155d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809115 | ||||||
| chr5:149809118 | GATAGATA others(50): Show |
G | 1 | a0001c0001t0002g0050 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.79-11154_79-11098d others(59): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809118 | ||||||
| chr5:149809122 | GATAGATA others(46): Show |
G | 38 | a0001c0001t0001g0053 a0001c0001t0001g0143 a0001c0001t0001g0240 others(35): Show |
38 | HG00408.hp2 HG00544.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.79-11268_79-11216d others(55): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809122 | ||||||
| chr5:149809122 | GATAGATA others(103): Show |
G | 7 | a0001c0001t0001g0228 a0001c0001t0007g0188 a0001c0004t0006g0210 others(4): Show |
7 | HG00280.hp2 HG02602.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-11268_79-11159d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809122 | ||||||
| chr5:149809126 | GATAGATA others(42): Show |
G | 37 | a0001c0001t0001g0069 a0001c0001t0001g0155 a0001c0001t0001g0186 others(34): Show |
37 | HG00738.hp2 HG01071.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.79-11268_79-11220d others(51): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809126 | ||||||
| chr5:149809126 | GATAGATA others(99): Show |
G | 5 | a0001c0001t0001g0220 a0001c0006t0001g0313 a0001c0006t0042g0001 others(2): Show |
5 | HG01496.hp2 HG03130.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-11268_79-11163d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809126 | ||||||
| chr5:149809130 | GATAGATA others(38): Show |
G | 9 | a0001c0001t0001g0181 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
9 | HG01361.hp2 HG01433.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-11268_79-11224d others(47): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809130 | ||||||
| chr5:149809130 | GATAGATA others(95): Show |
G | 1 | a0001c0006t0001g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79-11268_79-11167d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809130 | ||||||
| chr5:149809134 | G | GATAGATA others(205): Show |
1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.79-11269_79-11268i others(214): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809134 | ||||||
| chr5:149809134 | GATAGATA others(34): Show |
G | 2 | a0001c0001t0002g0282 a0001c0001t0015g0180 |
2 | HG01168.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.79-11268_79-11228d others(43): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809134 | ||||||
| chr5:149809172 | T | C | 7 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-11261T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809172 | |||||||
| chr5:149809175 | C | CATAG | 32 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0165 others(29): Show |
32 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.79-11215_79-11212d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809175 | ||||||
| chr5:149809175 | C | CATAGATA others(1): Show |
17 | a0001c0001t0001g0070 a0001c0001t0001g0206 a0001c0001t0001g0207 others(14): Show |
17 | HG00438.hp2 HG01928.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.79-11219_79-11212d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809175 | ||||||
| chr5:149809175 | C | CATAGATA others(5): Show |
9 | a0001c0001t0002g0154 a0001c0001t0002g0173 a0001c0001t0002g0194 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-11223_79-11212d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809175 | ||||||
| chr5:149809175 | CATAG | C | 8 | a0001c0001t0001g0098 a0001c0001t0002g0163 a0001c0006t0001g0099 others(5): Show |
8 | HG01243.hp1 HG01261.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-11215_79-11212d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809175 | ||||||
| chr5:149809175 | CATAGATA others(54): Show |
C | 1 | a0002c0002t0066g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.79-11215_79-11155d others(63): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809175 | ||||||
| chr5:149809179 | GATAGATA others(46): Show |
G | 20 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0149 others(17): Show |
20 | HG00280.hp1 HG00558.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.79-11211_79-11159d others(55): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809179 | ||||||
| chr5:149809179 | GATAGATA others(103): Show |
G | 1 | a0001c0001t0015g0300 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.79-11211_79-11102d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809179 | ||||||
| chr5:149809183 | GATAGATA others(42): Show |
G | 47 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0067 others(44): Show |
47 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.79-11211_79-11163d others(51): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809183 | ||||||
| chr5:149809187 | GATAGATA others(38): Show |
G | 22 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0094 others(19): Show |
22 | HG00140.hp1 HG00639.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.79-11211_79-11167d others(47): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809187 | ||||||
| chr5:149809191 | G | GATAGATA others(377): Show |
1 | a0002c0008t0005g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79-11212_79-11211i others(386): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809191 | ||||||
| chr5:149809191 | G | GATAGATA others(369): Show |
1 | a0005c0011t0001g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.79-11212_79-11211i others(378): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809191 | ||||||
| chr5:149809191 | GATAGATA others(34): Show |
G | 4 | a0001c0001t0044g0064 a0002c0014t0005g0259 a0002c0014t0005g0260 others(1): Show |
4 | HG02165.hp1 HG03491.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-11211_79-11171d others(43): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809191 | ||||||
| chr5:149809195 | GATAGATA others(30): Show |
G | 2 | a0001c0001t0003g0057 a0009c0020t0008g0004 |
2 | HG03195.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.79-11211_79-11175d others(39): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809195 | ||||||
| chr5:149809219 | GATCCATC others(6): Show |
G | 1 | a0007c0019t0017g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-11211_79-11199d others(15): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809219 | ||||||
| chr5:149809232 | C | CATAG | 34 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(31): Show |
34 | HG00408.hp2 HG01258.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.79-11158_79-11155d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809232 | C | CATAGATA others(1): Show |
17 | a0001c0001t0001g0258 a0001c0001t0001g0285 a0001c0001t0002g0154 others(14): Show |
17 | HG00408.hp1 HG00738.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.79-11162_79-11155d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809232 | C | CATAGATA others(5): Show |
1 | a0001c0001t0002g0282 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.79-11166_79-11155d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809232 | CATAG | C | 20 | a0001c0001t0001g0076 a0001c0001t0001g0155 a0001c0001t0001g0165 others(17): Show |
20 | HG00558.hp1 HG00741.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.79-11158_79-11155d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809232 | CATAGATA others(1): Show |
C | 11 | a0001c0001t0003g0167 a0001c0001t0020g0137 a0002c0002t0025g0027 others(8): Show |
11 | HG00738.hp1 HG01433.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-11162_79-11155d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809232 | CATAGATA others(9): Show |
C | 2 | a0008c0016t0026g0262 a0008c0016t0036g0122 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-11170_79-11155d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809232 | CATAGATA others(13): Show |
C | 2 | a0001c0004t0006g0095 a0001c0033t0001g0096 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.79-11174_79-11155d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809232 | CATAGATA others(54): Show |
C | 5 | a0001c0001t0002g0163 a0001c0001t0021g0140 a0001c0010t0038g0185 others(2): Show |
5 | HG00741.hp1 HG01261.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-11101_79-11041d others(63): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809232 | CATAGATA others(74): Show |
C | 25 | a0001c0001t0001g0201 a0001c0001t0001g0271 a0001c0001t0002g0148 others(22): Show |
25 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.79-11174_79-11094d others(83): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809232 | ||||||
| chr5:149809236 | GATAGATA others(46): Show |
G | 2 | a0001c0001t0003g0123 a0002c0008t0008g0191 |
2 | HG02523.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.79-11154_79-11102d others(55): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809236 | ||||||
| chr5:149809237 | A | ATAGATAG others(26): Show |
1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79-11175_79-11174i others(35): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809237 | ||||||
| chr5:149809240 | GATAGATA others(42): Show |
G | 2 | a0001c0001t0003g0087 a0001c0017t0006g0078 |
2 | HG02040.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.79-11154_79-11106d others(51): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809240 | ||||||
| chr5:149809241 | A | ATAGATAG others(22): Show |
1 | a0001c0009t0064g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.79-11175_79-11174i others(31): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809241 | ||||||
| chr5:149809243 | A | C | 1 | a0007c0019t0017g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-11190A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809243 | |||||||
| chr5:149809244 | G | C | 1 | a0007c0019t0017g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-11189G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809244 | |||||||
| chr5:149809244 | G | GATAGATA others(22): Show |
1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.79-11171_79-11170i others(31): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809244 | ||||||
| chr5:149809247 | A | C | 1 | a0007c0019t0017g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-11186A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809247 | |||||||
| chr5:149809248 | G | T | 1 | a0007c0019t0017g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-11185G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809248 | |||||||
| chr5:149809249 | A | C | 1 | a0007c0019t0017g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-11184A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809249 | |||||||
| chr5:149809252 | G | C | 1 | a0007c0019t0017g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-11181G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809252 | |||||||
| chr5:149809253 | A | ATAGATCC others(10): Show |
1 | a0007c0019t0017g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-11175_79-11174i others(19): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809253 | ||||||
| chr5:149809275 | A | C | 4 | a0001c0004t0024g0080 a0002c0008t0005g0129 a0005c0011t0001g0128 others(1): Show |
4 | HG00735.hp2 HG01884.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11158A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809275 | |||||||
| chr5:149809289 | C | CATAG | 20 | a0001c0001t0001g0149 a0001c0001t0001g0220 a0001c0001t0001g0240 others(17): Show |
20 | HG00280.hp1 HG00639.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.79-11097_79-11094d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAG | C | 86 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0062 others(83): Show |
86 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.79-11097_79-11094d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAGATA others(1): Show |
C | 40 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0098 others(37): Show |
40 | HG00408.hp1 HG01081.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.79-11101_79-11094d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAGATA others(5): Show |
C | 21 | a0001c0001t0001g0285 a0001c0001t0002g0173 a0001c0001t0002g0274 others(18): Show |
21 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.79-11105_79-11094d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAGATA others(9): Show |
C | 4 | a0001c0001t0002g0194 a0001c0004t0006g0095 a0001c0033t0001g0096 others(1): Show |
4 | HG04115.hp1 HG04199.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11109_79-11094d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAGATA others(13): Show |
C | 1 | a0002c0002t0010g0304 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.79-11113_79-11094d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAGATA others(17): Show |
C | 13 | a0001c0001t0003g0020 a0001c0001t0007g0176 a0001c0001t0007g0183 others(10): Show |
13 | HG01168.hp1 HG02293.hp2 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.79-11117_79-11094d others(26): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAGATA others(58): Show |
C | 1 | a0001c0001t0007g0025 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.79-11105_79-11041d others(67): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAGATA others(70): Show |
C | 6 | a0001c0001t0001g0165 a0001c0004t0018g0031 a0001c0004t0018g0034 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-11117_79-11041d others(79): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809289 | CATAGATA others(115): Show |
C | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79-11125_79-11004d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809289 | ||||||
| chr5:149809290 | A | G | 4 | a0001c0009t0009g0130 a0007c0019t0017g0315 a0008c0016t0026g0262 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11143A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809290 | |||||||
| chr5:149809293 | G | GATAGATA others(361): Show |
1 | a0001c0010t0001g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.79-11106_79-11105i others(370): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809293 | ||||||
| chr5:149809293 | G | GATAGATA others(353): Show |
1 | a0005c0011t0009g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79-11106_79-11105i others(362): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809293 | ||||||
| chr5:149809293 | G | GATAGATA others(353): Show |
1 | a0001c0010t0001g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.79-11106_79-11105i others(362): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809293 | ||||||
| chr5:149809293 | G | GATAGATA others(26): Show |
1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.79-11118_79-11117i others(35): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809293 | ||||||
| chr5:149809293 | GATAGATA others(50): Show |
G | 8 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0019g0072 others(5): Show |
8 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-11097_79-11041d others(59): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809293 | ||||||
| chr5:149809297 | G | GATAGATA others(349): Show |
1 | a0005c0011t0027g0132 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.79-11106_79-11105i others(358): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809297 | ||||||
| chr5:149809297 | G | GATAGATA others(353): Show |
1 | a0001c0010t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79-11106_79-11105i others(362): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809297 | ||||||
| chr5:149809297 | G | GATAGATA others(222): Show |
1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.79-11118_79-11117i others(231): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809297 | ||||||
| chr5:149809297 | GATAGATA others(99): Show |
G | 3 | a0001c0009t0009g0130 a0008c0016t0026g0262 a0008c0016t0036g0122 |
3 | HG02647.hp1 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-11109_79-11004d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809297 | ||||||
| chr5:149809301 | GATAGATA others(95): Show |
G | 1 | a0003c0003t0004g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.79-11105_79-11004d others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809301 | ||||||
| chr5:149809305 | GATAGATA others(91): Show |
G | 9 | a0002c0002t0025g0029 a0003c0003t0004g0150 a0003c0003t0004g0177 others(6): Show |
9 | HG00738.hp1 HG01433.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-11101_79-11004d others(100): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809305 | ||||||
| chr5:149809306 | A | G | 2 | a0001c0004t0006g0095 a0001c0033t0001g0096 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.79-11127A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809306 | |||||||
| chr5:149809309 | GATAGATA others(87): Show |
G | 2 | a0001c0001t0015g0189 a0002c0002t0025g0027 |
2 | HG00558.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.79-11097_79-11004d others(96): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809309 | ||||||
| chr5:149809313 | G | GATCCATC others(6): Show |
3 | a0001c0009t0064g0261 a0001c0030t0031g0320 a0007c0019t0017g0315 |
3 | HG03041.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.79-11118_79-11117i others(15): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809313 | ||||||
| chr5:149809336 | A | C | 2 | a0001c0001t0003g0182 a0001c0004t0024g0077 |
2 | HG02258.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.79-11097A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809336 | |||||||
| chr5:149809340 | CCATCTCT others(42): Show |
C | 1 | a0001c0001t0001g0070 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.79-11092_79-11044d others(51): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809340 | |||||||
| chr5:149809340 | CCATCTCT others(79): Show |
C | 1 | a0001c0009t0023g0218 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.79-11092_79-11007d others(88): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809340 | |||||||
| chr5:149809350 | C | CATAG | 22 | a0001c0001t0001g0083 a0001c0001t0001g0190 a0001c0001t0001g0280 others(19): Show |
22 | HG00609.hp1 HG00741.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.79-11044_79-11041d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809350 | ||||||
| chr5:149809350 | C | CATAGATA others(5): Show |
2 | a0001c0001t0001g0002 a0006c0007t0016g0035 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.79-11052_79-11041d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809350 | ||||||
| chr5:149809350 | CATAG | C | 18 | a0001c0001t0001g0098 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01168.hp2 HG01891.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-11044_79-11041d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809350 | ||||||
| chr5:149809350 | CATAGATA others(1): Show |
C | 32 | a0001c0001t0003g0020 a0001c0001t0003g0022 a0001c0001t0003g0024 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.79-11048_79-11041d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809350 | ||||||
| chr5:149809350 | CATAGATA others(5): Show |
C | 1 | a0001c0001t0015g0300 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.79-11052_79-11041d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809350 | ||||||
| chr5:149809350 | CATAGATA others(9): Show |
C | 13 | a0001c0001t0001g0220 a0001c0001t0001g0228 a0001c0001t0003g0182 others(10): Show |
13 | HG01496.hp2 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.79-11056_79-11041d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809350 | ||||||
| chr5:149809351 | A | G | 33 | a0001c0001t0001g0201 a0001c0001t0001g0271 a0001c0001t0002g0148 others(30): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.79-11082A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809351 | |||||||
| chr5:149809354 | GATAGATA others(42): Show |
G | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79-11052_79-11004d others(51): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809354 | ||||||
| chr5:149809354 | GATAGATA others(79): Show |
G | 2 | a0001c0004t0006g0095 a0001c0033t0001g0096 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.79-11052_79-10967d others(88): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809354 | ||||||
| chr5:149809358 | GATAGATA others(38): Show |
G | 29 | a0001c0001t0001g0201 a0001c0001t0001g0271 a0001c0001t0002g0148 others(26): Show |
29 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.79-11048_79-11004d others(47): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809358 | ||||||
| chr5:149809359 | A | G | 5 | a0001c0001t0003g0020 a0001c0004t0006g0107 a0001c0009t0046g0042 others(2): Show |
5 | HG02257.hp2 HG02976.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-11074A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809359 | |||||||
| chr5:149809362 | GATAGATA others(34): Show |
G | 4 | a0001c0004t0006g0112 a0001c0004t0006g0193 a0001c0006t0001g0099 others(1): Show |
4 | HG02293.hp2 HG02738.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11044_79-11004d others(43): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809362 | ||||||
| chr5:149809366 | GATAGATA others(30): Show |
G | 4 | a0001c0001t0001g0010 a0001c0004t0006g0115 a0003c0003t0033g0292 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-10966_79-10930d others(39): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809366 | ||||||
| chr5:149809370 | GATAGATA others(26): Show |
G | 3 | a0003c0003t0004g0287 a0003c0003t0004g0293 a0003c0003t0035g0297 |
3 | HG01943.hp1 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.79-11040_79-11008d others(35): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809370 | ||||||
| chr5:149809377 | A | C | 4 | a0001c0001t0020g0137 a0001c0004t0006g0210 a0001c0004t0030g0113 others(1): Show |
4 | HG00280.hp2 HG02273.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11056A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809377 | |||||||
| chr5:149809378 | G | C | 4 | a0001c0001t0020g0137 a0001c0004t0006g0210 a0001c0004t0030g0113 others(1): Show |
4 | HG00280.hp2 HG02273.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11055G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809378 | |||||||
| chr5:149809379 | A | ATCTCTAC others(2): Show |
4 | a0001c0001t0020g0137 a0001c0004t0006g0210 a0001c0004t0030g0113 others(1): Show |
4 | HG00280.hp2 HG02273.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11053_79-11052i others(11): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809379 | ||||||
| chr5:149809389 | A | AGATAGAT others(5): Show |
1 | a0002c0014t0005g0259 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.79-11041_79-11040i others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809389 | ||||||
| chr5:149809389 | A | AGATC | 8 | a0001c0001t0003g0057 a0001c0001t0003g0123 a0001c0001t0003g0156 others(5): Show |
8 | HG01106.hp2 HG01943.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-11043_79-11040d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809389 | ||||||
| chr5:149809389 | A | C | 55 | a0001c0001t0001g0143 a0001c0001t0001g0155 a0001c0001t0001g0161 others(52): Show |
55 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.79-11044A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809389 | |||||||
| chr5:149809390 | GATCCATC others(6): Show |
G | 4 | a0001c0001t0020g0137 a0001c0004t0006g0210 a0001c0004t0030g0113 others(1): Show |
4 | HG00280.hp2 HG02273.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-11040_79-11028d others(15): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809390 | ||||||
| chr5:149809403 | C | CATAG | 6 | a0001c0001t0001g0312 a0001c0004t0018g0034 a0001c0004t0018g0039 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-11007_79-11004d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809403 | ||||||
| chr5:149809403 | C | CGTAGATA others(1): Show |
11 | a0001c0001t0001g0220 a0001c0001t0001g0228 a0001c0001t0007g0188 others(8): Show |
11 | HG01496.hp2 HG02572.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-11030_79-11029i others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809403 | |||||||
| chr5:149809403 | CATAG | C | 19 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(16): Show |
19 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.79-11007_79-11004d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809403 | ||||||
| chr5:149809426 | A | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0280 a0004c0005t0001g0011 others(2): Show |
5 | HG00609.hp1 HG02280.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-11007A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809426 | |||||||
| chr5:149809438 | A | G | 1 | a0002c0008t0008g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.79-10995A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809438 | |||||||
| chr5:149809440 | C | CATAG | 4 | a0001c0001t0001g0062 a0001c0001t0001g0312 a0002c0002t0008g0030 others(1): Show |
4 | HG01975.hp2 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-10970_79-10967d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809440 | ||||||
| chr5:149809440 | CATAG | C | 19 | a0001c0001t0001g0240 a0001c0001t0003g0022 a0001c0001t0003g0024 others(16): Show |
19 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.79-10970_79-10967d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809440 | ||||||
| chr5:149809440 | CATAGATA others(34): Show |
C | 1 | a0001c0006t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.79-10966_79-10926d others(43): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809440 | ||||||
| chr5:149809440 | CATAGATA others(38): Show |
C | 3 | a0001c0001t0001g0285 a0001c0001t0002g0278 a0003c0003t0004g0294 |
3 | HG00738.hp2 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.79-10966_79-10922d others(47): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809440 | ||||||
| chr5:149809440 | CATAGATA others(42): Show |
C | 18 | a0001c0001t0002g0274 a0001c0001t0002g0275 a0001c0001t0002g0276 others(15): Show |
18 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.79-10966_79-10918d others(51): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809440 | ||||||
| chr5:149809440 | CATAGATA others(50): Show |
C | 3 | a0001c0001t0001g0190 a0001c0001t0003g0182 a0001c0001t0012g0048 |
3 | NA18943.hp1 NA18948.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.79-10966_79-10910d others(59): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809440 | ||||||
| chr5:149809444 | GATAGATA others(26): Show |
G | 7 | a0001c0001t0003g0020 a0001c0004t0006g0107 a0001c0009t0046g0042 others(4): Show |
7 | HG02257.hp2 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-10966_79-10934d others(35): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809444 | ||||||
| chr5:149809477 | C | CATAG | 21 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0062 others(18): Show |
21 | HG01081.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.79-10908_79-10905d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809477 | ||||||
| chr5:149809477 | C | CATAGATA others(1): Show |
3 | a0001c0001t0044g0064 a0001c0024t0001g0091 a0003c0003t0011g0237 |
3 | HG02148.hp1 HG03491.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.79-10912_79-10905d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809477 | ||||||
| chr5:149809477 | CATAG | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0070 others(70): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.79-10908_79-10905d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809477 | ||||||
| chr5:149809477 | CATAGATA others(1): Show |
C | 35 | a0001c0001t0001g0018 a0001c0001t0001g0053 a0001c0001t0001g0074 others(32): Show |
35 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.79-10912_79-10905d others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809477 | ||||||
| chr5:149809477 | CATAGATA others(5): Show |
C | 5 | a0001c0001t0023g0229 a0001c0001t0045g0198 a0002c0008t0008g0319 others(2): Show |
5 | HG01943.hp1 HG02735.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-10916_79-10905d others(14): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809477 | ||||||
| chr5:149809477 | CATAGATA others(9): Show |
C | 10 | a0001c0001t0001g0143 a0001c0001t0001g0221 a0001c0001t0003g0026 others(7): Show |
10 | HG00544.hp2 HG00735.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-10920_79-10905d others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809477 | ||||||
| chr5:149809477 | CATAGATA others(13): Show |
C | 41 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0181 others(38): Show |
41 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.79-10924_79-10905d others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809477 | ||||||
| chr5:149809477 | CATAGATA others(17): Show |
C | 2 | a0001c0010t0056g0153 a0001c0017t0006g0078 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.79-10928_79-10905d others(26): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809477 | ||||||
| chr5:149809481 | G | GATAGATA others(26): Show |
1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.79-10930_79-10929i others(35): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809481 | ||||||
| chr5:149809612 | C | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0194 |
2 | NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.79-10821C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809612 | |||||||
| chr5:149809613 | G | A | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79-10820G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809613 | |||||||
| chr5:149809687 | T | TA | 10 | a0001c0001t0002g0208 a0001c0001t0003g0135 a0001c0001t0003g0272 others(7): Show |
10 | HG01934.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-10719dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809687 | ||||||
| chr5:149809687 | TA | T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0143 a0001c0001t0001g0181 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.79-10719delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809687 | ||||||
| chr5:149809687 | TAA | T | 8 | a0001c0001t0003g0024 a0001c0001t0009g0142 a0001c0018t0029g0197 others(5): Show |
8 | HG00280.hp1 HG01074.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-10720_79-10719d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809687 | ||||||
| chr5:149809687 | TAAA | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0312 a0001c0001t0040g0065 others(8): Show |
11 | HG01069.hp1 HG01891.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-10721_79-10719d others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809687 | ||||||
| chr5:149809687 | TAAAA | T | 136 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(133): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.79-10722_79-10719d others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809687 | ||||||
| chr5:149809687 | TAAAAA | T | 19 | a0001c0001t0015g0232 a0001c0004t0006g0101 a0001c0004t0006g0102 others(16): Show |
19 | HG01168.hp1 HG01978.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.79-10723_79-10719d others(7): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149809687 | ||||||
| chr5:149809748 | A | C | 2 | a0002c0002t0005g0028 a0002c0002t0008g0030 |
2 | HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.79-10685A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809748 | |||||||
| chr5:149809781 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.79-10652G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809781 | |||||||
| chr5:149809797 | A | G | 9 | a0001c0009t0064g0261 a0001c0018t0029g0197 a0001c0018t0029g0217 others(6): Show |
9 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-10636A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809797 | |||||||
| chr5:149809808 | G | A | 1 | a0002c0008t0008g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-10625G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809808 | |||||||
| chr5:149809886 | G | C | 35 | a0001c0001t0001g0098 a0001c0001t0001g0155 a0001c0001t0001g0190 others(32): Show |
35 | HG00558.hp1 HG01433.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.79-10547G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809886 | |||||||
| chr5:149809915 | T | C | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-10518T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809915 | |||||||
| chr5:149809926 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(258): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.79-10507G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149809926 | |||||||
| chr5:149810053 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.79-10380G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149810053 | |||||||
| chr5:149810396 | C | T | 10 | a0001c0001t0002g0173 a0001c0009t0064g0261 a0001c0010t0001g0056 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.79-10037C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149810396 | |||||||
| chr5:149810434 | A | G | 201 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0053 others(198): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.79-9999A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149810434 | |||||||
| chr5:149810521 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.79-9912C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149810521 | |||||||
| chr5:149810583 | G | A | 1 | a0001c0001t0003g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.79-9850G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149810583 | |||||||
| chr5:149810685 | C | G | 24 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(21): Show |
24 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.79-9748C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149810685 | |||||||
| chr5:149810809 | G | A | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-9624G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149810809 | |||||||
| chr5:149811091 | C | T | 1 | a0003c0003t0004g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.79-9342C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811091 | |||||||
| chr5:149811225 | T | G | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-9208T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811225 | |||||||
| chr5:149811236 | G | A | 25 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(22): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.79-9197G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811236 | |||||||
| chr5:149811247 | C | T | 33 | a0001c0017t0017g0014 a0003c0003t0004g0045 a0003c0003t0004g0150 others(30): Show |
33 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.79-9186C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811247 | |||||||
| chr5:149811287 | C | T | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.79-9146C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811287 | |||||||
| chr5:149811435 | C | T | 2 | a0001c0001t0012g0085 a0001c0001t0012g0090 |
2 | NA18964.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.79-8998C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811435 | |||||||
| chr5:149811437 | T | C | 2 | a0001c0010t0038g0185 a0001c0010t0056g0153 |
2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.79-8996T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811437 | |||||||
| chr5:149811548 | C | T | 159 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0240 others(156): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.79-8885C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811548 | |||||||
| chr5:149811953 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.79-8480C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811953 | |||||||
| chr5:149811984 | C | T | 41 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(38): Show |
41 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.79-8449C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811984 | |||||||
| chr5:149811986 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.79-8447G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149811986 | |||||||
| chr5:149812089 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.79-8344A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812089 | |||||||
| chr5:149812118 | A | T | 4 | a0002c0008t0008g0015 a0002c0008t0008g0191 a0002c0008t0008g0319 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-8315A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812118 | |||||||
| chr5:149812154 | G | A | 1 | a0002c0002t0025g0286 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.79-8279G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812154 | |||||||
| chr5:149812293 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.79-8140T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812293 | |||||||
| chr5:149812441 | ATAAGG | A | 41 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(38): Show |
41 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.79-7987_79-7983del others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149812441 | ||||||
| chr5:149812473 | T | C | 8 | a0001c0001t0002g0050 a0001c0001t0002g0205 a0001c0001t0002g0208 others(5): Show |
8 | HG00408.hp1 HG00438.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-7960T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812473 | |||||||
| chr5:149812603 | T | C | 48 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(45): Show |
48 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.79-7830T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812603 | |||||||
| chr5:149812638 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.79-7795C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812638 | |||||||
| chr5:149812912 | A | G | 1 | a0001c0001t0002g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.79-7521A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812912 | |||||||
| chr5:149812993 | A | G | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.79-7440A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149812993 | |||||||
| chr5:149813040 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79-7393G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813040 | |||||||
| chr5:149813041 | G | A | 7 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-7392G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813041 | |||||||
| chr5:149813109 | T | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0312 a0002c0008t0008g0015 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-7324T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813109 | |||||||
| chr5:149813181 | G | T | 41 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(38): Show |
41 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.79-7252G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813181 | |||||||
| chr5:149813231 | GA | G | 3 | a0001c0004t0006g0104 a0001c0004t0006g0105 a0001c0004t0006g0107 |
3 | NA18974.hp1 NA19070.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.79-7201delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813231 | |||||||
| chr5:149813283 | A | G | 152 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0165 others(149): Show |
152 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(149): Show |
intron_variant | MODIFIER | c.79-7150A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813283 | |||||||
| chr5:149813286 | A | G | 1 | a0002c0008t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79-7147A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813286 | |||||||
| chr5:149813502 | C | T | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.79-6931C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813502 | |||||||
| chr5:149813570 | C | T | 32 | a0001c0017t0017g0014 a0003c0003t0004g0045 a0003c0003t0004g0150 others(29): Show |
32 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.79-6863C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813570 | |||||||
| chr5:149813860 | C | T | 1 | a0002c0008t0071g0184 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.79-6573C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149813860 | |||||||
| chr5:149814419 | T | G | 2 | a0008c0016t0026g0009 a0008c0016t0026g0262 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-6014T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149814419 | |||||||
| chr5:149814445 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0312 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.79-5988G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149814445 | |||||||
| chr5:149814495 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0312 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.79-5938G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149814495 | |||||||
| chr5:149814791 | C | G | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-5642C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149814791 | |||||||
| chr5:149814836 | A | G | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.79-5597A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149814836 | |||||||
| chr5:149814844 | G | A | 7 | a0002c0002t0005g0006 a0002c0002t0005g0212 a0002c0002t0008g0003 others(4): Show |
7 | HG02451.hp2 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-5589G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149814844 | |||||||
| chr5:149814894 | C | T | 1 | a0004c0005t0001g0257 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.79-5539C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149814894 | |||||||
| chr5:149814922 | C | T | 108 | a0001c0001t0001g0165 a0001c0001t0001g0240 a0001c0001t0001g0312 others(105): Show |
108 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.79-5511C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149814922 | |||||||
| chr5:149815222 | G | A | 41 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(38): Show |
41 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.79-5211G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149815222 | |||||||
| chr5:149815360 | T | C | 160 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0165 others(157): Show |
160 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(157): Show |
intron_variant | MODIFIER | c.79-5073T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149815360 | |||||||
| chr5:149815538 | AATTT | A | 32 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(29): Show |
32 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.79-4881_79-4878del others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149815538 | ||||||
| chr5:149815562 | T | G | 68 | a0001c0001t0001g0165 a0001c0001t0001g0240 a0001c0001t0001g0312 others(65): Show |
68 | HG00280.hp2 HG00639.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.79-4871T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149815562 | |||||||
| chr5:149815746 | C | T | 1 | a0003c0012t0014g0110 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.79-4687C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149815746 | |||||||
| chr5:149815826 | T | C | 164 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0165 others(161): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.79-4607T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149815826 | |||||||
| chr5:149815828 | T | C | 1 | a0002c0002t0068g0250 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79-4605T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149815828 | |||||||
| chr5:149815884 | C | T | 9 | a0003c0003t0004g0247 a0003c0003t0004g0305 a0003c0003t0011g0063 others(6): Show |
9 | HG01928.hp2 HG01952.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-4549C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149815884 | |||||||
| chr5:149815991 | G | C | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-4442G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149815991 | |||||||
| chr5:149816015 | G | A | 1 | a0004c0005t0001g0257 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.79-4418G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816015 | |||||||
| chr5:149816036 | G | A | 2 | a0002c0002t0005g0028 a0010c0021t0061g0311 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.79-4397G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816036 | |||||||
| chr5:149816040 | C | G | 116 | a0001c0001t0001g0165 a0001c0001t0001g0240 a0001c0001t0001g0312 others(113): Show |
116 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.79-4393C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816040 | |||||||
| chr5:149816050 | CA | C | 8 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-4382delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816050 | |||||||
| chr5:149816149 | C | A | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-4284C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816149 | |||||||
| chr5:149816163 | C | T | 41 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(38): Show |
41 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.79-4270C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816163 | |||||||
| chr5:149816338 | G | A | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-4095G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816338 | |||||||
| chr5:149816361 | G | A | 1 | a0001c0033t0001g0096 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.79-4072G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816361 | |||||||
| chr5:149816494 | G | T | 8 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-3939G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816494 | |||||||
| chr5:149816527 | A | C | 120 | a0001c0001t0001g0165 a0001c0001t0001g0240 a0001c0001t0001g0312 others(117): Show |
120 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.79-3906A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816527 | |||||||
| chr5:149816660 | T | G | 1 | a0007c0023t0017g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79-3773T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816660 | |||||||
| chr5:149816671 | G | C | 120 | a0001c0001t0001g0165 a0001c0001t0001g0240 a0001c0001t0001g0312 others(117): Show |
120 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.79-3762G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816671 | |||||||
| chr5:149816743 | T | C | 1 | a0005c0013t0009g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.79-3690T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816743 | |||||||
| chr5:149816766 | G | A | 83 | a0001c0001t0001g0165 a0001c0001t0001g0240 a0001c0001t0001g0312 others(80): Show |
83 | HG00280.hp2 HG00639.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.79-3667G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816766 | |||||||
| chr5:149816950 | A | G | 45 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(42): Show |
45 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.79-3483A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149816950 | |||||||
| chr5:149817001 | C | T | 20 | a0001c0001t0001g0240 a0001c0001t0057g0238 a0002c0002t0068g0250 others(17): Show |
20 | HG00639.hp2 HG01106.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.79-3432C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817001 | |||||||
| chr5:149817075 | C | T | 45 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(42): Show |
45 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.79-3358C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817075 | |||||||
| chr5:149817084 | T | TGG | 8 | a0001c0001t0002g0050 a0001c0001t0002g0205 a0001c0001t0002g0208 others(5): Show |
8 | HG00408.hp1 HG00438.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-3347_79-3346dup others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149817084 | ||||||
| chr5:149817119 | T | G | 160 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0165 others(157): Show |
160 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(157): Show |
intron_variant | MODIFIER | c.79-3314T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817119 | |||||||
| chr5:149817135 | A | G | 1 | a0003c0003t0004g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.79-3298A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817135 | |||||||
| chr5:149817353 | A | G | 45 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(42): Show |
45 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.79-3080A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817353 | |||||||
| chr5:149817496 | G | A | 8 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-2937G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817496 | |||||||
| chr5:149817614 | T | C | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.79-2819T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817614 | |||||||
| chr5:149817667 | T | C | 75 | a0001c0001t0001g0165 a0001c0001t0001g0240 a0001c0001t0001g0312 others(72): Show |
75 | HG00280.hp2 HG00639.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.79-2766T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817667 | |||||||
| chr5:149817916 | C | T | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-2517C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817916 | |||||||
| chr5:149817988 | G | A | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-2445G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817988 | |||||||
| chr5:149817989 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.79-2444G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149817989 | |||||||
| chr5:149818017 | G | A | 7 | a0001c0017t0017g0014 a0006c0007t0016g0012 a0006c0007t0016g0040 others(4): Show |
7 | HG02572.hp1 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-2416G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818017 | |||||||
| chr5:149818046 | T | C | 52 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(49): Show |
52 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(49): Show |
intron_variant | MODIFIER | c.79-2387T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818046 | |||||||
| chr5:149818068 | C | T | 4 | a0002c0008t0008g0015 a0002c0008t0008g0191 a0002c0008t0008g0319 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-2365C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818068 | |||||||
| chr5:149818132 | G | A | 2 | a0013c0027t0037g0318 a0014c0025t0031g0043 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-2301G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818132 | |||||||
| chr5:149818184 | C | G | 25 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(22): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.79-2249C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818184 | |||||||
| chr5:149818216 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0312 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.79-2217T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818216 | |||||||
| chr5:149818252 | T | C | 52 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(49): Show |
52 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(49): Show |
intron_variant | MODIFIER | c.79-2181T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818252 | |||||||
| chr5:149818284 | T | C | 4 | a0002c0008t0008g0015 a0002c0008t0008g0191 a0002c0008t0008g0319 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-2149T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818284 | |||||||
| chr5:149818327 | G | C | 5 | a0001c0006t0001g0316 a0002c0008t0071g0184 a0007c0019t0017g0314 others(2): Show |
5 | HG02257.hp2 HG02895.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-2106G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818327 | |||||||
| chr5:149818361 | A | G | 1 | a0003c0012t0014g0120 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.79-2072A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818361 | |||||||
| chr5:149818488 | C | A | 4 | a0002c0008t0008g0015 a0002c0008t0008g0191 a0002c0008t0008g0319 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-1945C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818488 | |||||||
| chr5:149818496 | C | T | 1 | a0006c0007t0016g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.79-1937C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818496 | |||||||
| chr5:149818497 | G | T | 25 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(22): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.79-1936G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818497 | |||||||
| chr5:149818543 | C | A | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-1890C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149818543 | |||||||
| chr5:149819060 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.79-1373A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819060 | |||||||
| chr5:149819470 | GTGTT | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0165 others(97): Show |
100 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.79-945_79-942delGT others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149819470 | ||||||
| chr5:149819476 | GTTTGTTT others(17): Show |
G | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.79-945_79-922delGT others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149819476 | ||||||
| chr5:149819482 | TTG | T | 5 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-949_79-948delGT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149819482 | ||||||
| chr5:149819485 | TTTG | T | 11 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0002c0002t0005g0016 others(8): Show |
11 | HG01261.hp2 HG04184.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-945_79-943delGT others(1): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149819485 | ||||||
| chr5:149819493 | T | G | 11 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0002c0002t0005g0016 others(8): Show |
11 | HG01261.hp2 HG04184.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-940T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819493 | |||||||
| chr5:149819494 | G | GT | 25 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(22): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.79-930dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149819494 | ||||||
| chr5:149819494 | G | T | 11 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0002c0002t0005g0016 others(8): Show |
11 | HG01261.hp2 HG04184.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-939G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819494 | |||||||
| chr5:149819495 | T | G | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.79-938T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819495 | |||||||
| chr5:149819498 | T | G | 8 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-935T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819498 | |||||||
| chr5:149819514 | C | T | 43 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(40): Show |
43 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.79-919C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819514 | |||||||
| chr5:149819585 | G | A | 70 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0240 others(67): Show |
70 | HG00280.hp2 HG00639.hp2 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.79-848G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819585 | |||||||
| chr5:149819598 | G | T | 2 | a0002c0002t0005g0016 a0003c0003t0052g0192 |
2 | NA19012.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.79-835G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819598 | |||||||
| chr5:149819757 | C | T | 35 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(32): Show |
35 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.79-676C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819757 | |||||||
| chr5:149819762 | C | T | 7 | a0002c0002t0005g0006 a0002c0002t0005g0212 a0002c0002t0008g0003 others(4): Show |
7 | HG02451.hp2 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-671C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819762 | |||||||
| chr5:149819904 | C | T | 25 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(22): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.79-529C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149819904 | |||||||
| chr5:149820011 | C | CA | 111 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0165 others(108): Show |
111 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.79-421dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 149820011 | ||||||
| chr5:149820093 | C | T | 20 | a0001c0001t0001g0240 a0001c0001t0057g0238 a0002c0002t0068g0250 others(17): Show |
20 | HG00639.hp2 HG01106.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.79-340C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149820093 | |||||||
| chr5:149820145 | A | G | 1 | a0001c0001t0003g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.79-288A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149820145 | |||||||
| chr5:149820157 | T | C | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-276T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149820157 | |||||||
| chr5:149820230 | A | G | 1 | a0001c0004t0024g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79-203A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149820230 | |||||||
| chr5:149820252 | C | T | 1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-181C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149820252 | |||||||
| chr5:149820326 | G | A | 45 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(42): Show |
45 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.79-107G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 1/11 | chr5 | 149820326 | |||||||
| chr5:149820728 | CAA | C | 39 | a0001c0017t0017g0014 a0002c0002t0005g0006 a0002c0002t0005g0212 others(36): Show |
39 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.252+124_252+125del others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 149820728 | ||||||
| chr5:149820839 | A | G | 21 | a0001c0001t0001g0240 a0001c0001t0057g0238 a0002c0002t0008g0030 others(18): Show |
21 | HG00639.hp2 HG01106.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.252+233A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149820839 | |||||||
| chr5:149820890 | G | C | 8 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+284G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149820890 | |||||||
| chr5:149821040 | T | C | 162 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0165 others(159): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.252+434T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149821040 | |||||||
| chr5:149821080 | G | A | 1 | a0001c0004t0006g0105 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.252+474G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149821080 | |||||||
| chr5:149821357 | A | G | 53 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(50): Show |
53 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.252+751A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149821357 | |||||||
| chr5:149821369 | G | A | 25 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(22): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.252+763G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149821369 | |||||||
| chr5:149821619 | C | T | 1 | a0002c0014t0005g0017 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.252+1013C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149821619 | |||||||
| chr5:149821702 | C | T | 4 | a0002c0002t0005g0168 a0002c0002t0010g0038 a0002c0002t0032g0041 others(1): Show |
4 | NA18941.hp2 NA18994.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+1096C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149821702 | |||||||
| chr5:149821754 | C | T | 1 | a0002c0002t0025g0286 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.252+1148C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149821754 | |||||||
| chr5:149822107 | A | G | 42 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(39): Show |
42 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.252+1501A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822107 | |||||||
| chr5:149822295 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.252+1689A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822295 | |||||||
| chr5:149822319 | G | C | 1 | a0001c0004t0030g0253 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.252+1713G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822319 | |||||||
| chr5:149822320 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.252+1714C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822320 | |||||||
| chr5:149822393 | C | G | 13 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(10): Show |
13 | HG01433.hp1 HG01496.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.252+1787C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822393 | |||||||
| chr5:149822553 | G | T | 2 | a0001c0001t0023g0229 a0001c0001t0041g0222 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.252+1947G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822553 | |||||||
| chr5:149822605 | A | G | 45 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(42): Show |
45 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.252+1999A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822605 | |||||||
| chr5:149822643 | C | G | 162 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0165 others(159): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.252+2037C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822643 | |||||||
| chr5:149822705 | C | A | 42 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(39): Show |
42 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.252+2099C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822705 | |||||||
| chr5:149822706 | G | A | 32 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(29): Show |
32 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.252+2100G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822706 | |||||||
| chr5:149822844 | C | G | 1 | a0004c0005t0001g0246 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.252+2238C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822844 | |||||||
| chr5:149822860 | G | GGAGCCCA others(8): Show |
5 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+2259_252+2260i others(17): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 149822860 | ||||||
| chr5:149822920 | A | G | 1 | a0001c0001t0012g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.252+2314A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822920 | |||||||
| chr5:149822950 | C | T | 4 | a0001c0004t0006g0101 a0001c0004t0006g0104 a0001c0004t0006g0105 others(1): Show |
4 | NA18974.hp1 NA19070.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+2344C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822950 | |||||||
| chr5:149822955 | T | A | 1 | a0004c0005t0001g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.252+2349T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149822955 | |||||||
| chr5:149823060 | C | T | 1 | a0001c0010t0009g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.252+2454C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823060 | |||||||
| chr5:149823222 | G | A | 4 | a0001c0001t0021g0140 a0001c0001t0021g0146 a0001c0001t0021g0225 others(1): Show |
4 | HG00741.hp1 HG01258.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+2616G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823222 | |||||||
| chr5:149823330 | G | A | 34 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(31): Show |
34 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.252+2724G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823330 | |||||||
| chr5:149823502 | C | T | 1 | a0001c0017t0017g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.252+2896C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823502 | |||||||
| chr5:149823524 | G | A | 1 | a0001c0001t0020g0299 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.252+2918G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823524 | |||||||
| chr5:149823526 | A | T | 1 | a0001c0001t0020g0299 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.252+2920A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823526 | |||||||
| chr5:149823530 | T | G | 1 | a0001c0001t0020g0299 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.252+2924T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823530 | |||||||
| chr5:149823535 | G | T | 1 | a0001c0001t0020g0299 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.252+2929G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823535 | |||||||
| chr5:149823536 | T | G | 1 | a0001c0001t0020g0299 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.252+2930T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823536 | |||||||
| chr5:149823598 | T | C | 2 | a0001c0001t0002g0278 a0001c0001t0002g0307 |
2 | HG00738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.252+2992T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823598 | |||||||
| chr5:149823743 | T | G | 1 | a0001c0001t0012g0124 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.253-2930T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823743 | |||||||
| chr5:149823787 | G | C | 42 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(39): Show |
42 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.253-2886G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823787 | |||||||
| chr5:149823910 | T | G | 4 | a0001c0004t0018g0034 a0001c0004t0018g0039 a0001c0004t0024g0077 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-2763T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823910 | |||||||
| chr5:149823999 | C | T | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.253-2674C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149823999 | |||||||
| chr5:149824029 | T | C | 1 | a0001c0024t0001g0091 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.253-2644T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824029 | |||||||
| chr5:149824072 | C | A | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.253-2601C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824072 | |||||||
| chr5:149824143 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.253-2530G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824143 | |||||||
| chr5:149824219 | A | G | 25 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(22): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.253-2454A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824219 | |||||||
| chr5:149824228 | G | A | 2 | a0003c0003t0004g0290 a0003c0003t0004g0291 |
2 | NA18962.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.253-2445G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824228 | |||||||
| chr5:149824232 | C | T | 5 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-2441C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824232 | |||||||
| chr5:149824242 | TC | T | 3 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 |
3 | HG02109.hp2 HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.253-2428delC | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 149824242 | ||||||
| chr5:149824430 | A | G | 45 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(42): Show |
45 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.253-2243A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824430 | |||||||
| chr5:149824438 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0242 a0003c0003t0004g0294 |
3 | HG01346.hp1 HG01496.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.253-2235A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824438 | |||||||
| chr5:149824601 | C | T | 1 | a0001c0009t0064g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-2072C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824601 | |||||||
| chr5:149824614 | G | A | 1 | a0002c0008t0063g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.253-2059G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824614 | |||||||
| chr5:149824722 | G | A | 4 | a0001c0006t0001g0316 a0007c0019t0017g0314 a0007c0019t0017g0315 others(1): Show |
4 | HG02257.hp2 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-1951G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824722 | |||||||
| chr5:149824732 | G | A | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.253-1941G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824732 | |||||||
| chr5:149824772 | C | T | 1 | a0009c0020t0008g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.253-1901C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824772 | |||||||
| chr5:149824881 | C | T | 62 | a0001c0001t0001g0165 a0001c0001t0001g0312 a0001c0004t0006g0095 others(59): Show |
62 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.253-1792C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824881 | |||||||
| chr5:149824898 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0062 others(64): Show |
67 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.253-1775C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149824898 | |||||||
| chr5:149824965 | CA | C | 6 | a0002c0002t0008g0030 a0002c0008t0008g0015 a0002c0008t0008g0191 others(3): Show |
6 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-1704delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 149824965 | ||||||
| chr5:149825049 | G | T | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.253-1624G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825049 | |||||||
| chr5:149825082 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.253-1591G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825082 | |||||||
| chr5:149825172 | G | A | 42 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(39): Show |
42 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.253-1501G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825172 | |||||||
| chr5:149825214 | A | G | 1 | a0001c0004t0030g0253 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.253-1459A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825214 | |||||||
| chr5:149825257 | G | C | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.253-1416G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825257 | |||||||
| chr5:149825266 | G | A | 1 | a0003c0003t0004g0281 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.253-1407G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825266 | |||||||
| chr5:149825289 | C | G | 52 | a0001c0001t0001g0240 a0001c0001t0057g0238 a0001c0017t0017g0014 others(49): Show |
52 | HG00140.hp2 HG00639.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.253-1384C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825289 | |||||||
| chr5:149825301 | C | A | 1 | a0004c0005t0012g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.253-1372C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825301 | |||||||
| chr5:149825309 | A | G | 1 | a0005c0013t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.253-1364A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825309 | |||||||
| chr5:149825326 | C | A | 7 | a0001c0001t0045g0198 a0002c0002t0008g0030 a0002c0008t0008g0015 others(4): Show |
7 | HG02145.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-1347C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825326 | |||||||
| chr5:149825437 | C | G | 8 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-1236C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825437 | |||||||
| chr5:149825579 | A | G | 4 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 others(1): Show |
4 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-1094A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825579 | |||||||
| chr5:149825630 | C | T | 1 | a0001c0001t0003g0273 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.253-1043C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825630 | |||||||
| chr5:149825854 | C | A | 76 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(73): Show |
76 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.253-819C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149825854 | |||||||
| chr5:149826032 | T | C | 13 | a0001c0001t0045g0198 a0001c0004t0018g0031 a0001c0004t0018g0034 others(10): Show |
13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.253-641T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826032 | |||||||
| chr5:149826067 | G | T | 150 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0045g0198 others(147): Show |
150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.253-606G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826067 | |||||||
| chr5:149826314 | C | T | 33 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(30): Show |
33 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.253-359C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826314 | |||||||
| chr5:149826340 | A | G | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.253-333A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826340 | |||||||
| chr5:149826341 | G | A | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.253-332G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826341 | |||||||
| chr5:149826377 | G | A | 32 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0047g0265 others(29): Show |
32 | HG00609.hp2 HG00738.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.253-296G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826377 | |||||||
| chr5:149826392 | G | A | 1 | a0003c0012t0014g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.253-281G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826392 | |||||||
| chr5:149826405 | C | T | 1 | a0004c0005t0001g0248 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.253-268C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826405 | |||||||
| chr5:149826429 | G | A | 31 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(28): Show |
31 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.253-244G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826429 | |||||||
| chr5:149826434 | C | T | 2 | a0002c0002t0005g0081 a0002c0002t0032g0263 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.253-239C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826434 | |||||||
| chr5:149826436 | A | G | 3 | a0002c0002t0010g0060 a0002c0002t0010g0204 a0002c0002t0010g0264 |
3 | NA18943.hp2 NA19058.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.253-237A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826436 | |||||||
| chr5:149826541 | G | A | 37 | a0001c0001t0045g0198 a0001c0001t0047g0265 a0002c0002t0005g0016 others(34): Show |
37 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.253-132G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826541 | |||||||
| chr5:149826630 | C | A | 1 | a0006c0007t0060g0032 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.253-43C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 2/11 | chr5 | 149826630 | |||||||
| chr5:149826944 | A | C | 1 | a0001c0017t0017g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.465+59A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149826944 | |||||||
| chr5:149826967 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.465+82C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149826967 | |||||||
| chr5:149826968 | G | A | 31 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(28): Show |
31 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.465+83G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149826968 | |||||||
| chr5:149826991 | G | A | 1 | a0001c0004t0006g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.465+106G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149826991 | |||||||
| chr5:149827010 | G | T | 15 | a0002c0008t0005g0129 a0004c0005t0001g0011 a0004c0005t0001g0121 others(12): Show |
15 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.465+125G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827010 | |||||||
| chr5:149827044 | G | C | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+159G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827044 | |||||||
| chr5:149827068 | A | G | 1 | a0001c0009t0009g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.465+183A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827068 | |||||||
| chr5:149827275 | C | G | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.465+390C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827275 | |||||||
| chr5:149827291 | C | G | 7 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.465+406C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827291 | |||||||
| chr5:149827427 | C | T | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.465+542C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827427 | |||||||
| chr5:149827428 | G | A | 1 | a0001c0004t0018g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.465+543G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827428 | |||||||
| chr5:149827593 | C | A | 33 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0002c0002t0005g0016 others(30): Show |
33 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.465+708C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827593 | |||||||
| chr5:149827702 | A | G | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.465+817A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827702 | |||||||
| chr5:149827711 | C | T | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.465+826C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827711 | |||||||
| chr5:149827721 | G | T | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.465+836G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149827721 | |||||||
| chr5:149828213 | A | T | 1 | a0002c0002t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.465+1328A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149828213 | |||||||
| chr5:149828320 | T | G | 1 | a0003c0012t0014g0120 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.465+1435T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149828320 | |||||||
| chr5:149828397 | A | G | 1 | a0003c0003t0035g0297 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.465+1512A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149828397 | |||||||
| chr5:149828418 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.465+1533G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149828418 | |||||||
| chr5:149828769 | G | C | 6 | a0001c0001t0045g0198 a0001c0030t0031g0320 a0008c0016t0026g0009 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+1884G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149828769 | |||||||
| chr5:149828880 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.466-1887A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149828880 | |||||||
| chr5:149828883 | AT | A | 46 | a0001c0001t0001g0047 a0001c0001t0023g0229 a0001c0001t0045g0198 others(43): Show |
46 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.466-1869delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149828883 | ||||||
| chr5:149828899 | A | T | 1 | a0001c0001t0015g0232 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.466-1868A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149828899 | |||||||
| chr5:149828953 | G | T | 39 | a0001c0001t0045g0198 a0001c0017t0017g0014 a0001c0018t0029g0197 others(36): Show |
39 | HG00140.hp2 HG00280.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.466-1814G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149828953 | |||||||
| chr5:149829205 | A | G | 49 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(46): Show |
49 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.466-1562A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829205 | |||||||
| chr5:149829272 | C | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0010 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.466-1495C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829272 | |||||||
| chr5:149829316 | A | C | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.466-1451A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829316 | |||||||
| chr5:149829554 | C | G | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0226 |
3 | HG00438.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.466-1213C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829554 | |||||||
| chr5:149829679 | G | A | 10 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 others(7): Show |
10 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-1088G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829679 | |||||||
| chr5:149829688 | G | GA | 9 | a0001c0001t0003g0057 a0001c0001t0003g0182 a0001c0001t0045g0198 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.466-1065dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149829688 | ||||||
| chr5:149829774 | G | A | 1 | a0001c0017t0006g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.466-993G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829774 | |||||||
| chr5:149829872 | C | T | 7 | a0001c0001t0001g0062 a0001c0001t0001g0083 a0001c0001t0001g0155 others(4): Show |
7 | HG00558.hp1 HG01106.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-895C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829872 | |||||||
| chr5:149829949 | C | T | 2 | a0001c0009t0064g0261 a0002c0002t0008g0030 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.466-818C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829949 | |||||||
| chr5:149829983 | C | T | 146 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(143): Show |
146 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.466-784C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149829983 | |||||||
| chr5:149830009 | T | G | 49 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(46): Show |
49 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.466-758T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830009 | |||||||
| chr5:149830030 | C | CA | 14 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0220 others(11): Show |
14 | HG01928.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.466-713dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830030 | ||||||
| chr5:149830030 | C | CAAAAAAA others(9): Show |
1 | a0013c0027t0037g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.466-728_466-713dup others(16): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830030 | ||||||
| chr5:149830033 | AAAAAAAA others(15): Show |
A | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.466-718_466-697del others(22): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830033 | ||||||
| chr5:149830037 | AAAAAAAA others(11): Show |
A | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.466-714_466-697del others(18): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830037 | ||||||
| chr5:149830042 | AAAAAAAA others(6): Show |
A | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.466-712_466-700del others(13): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830042 | ||||||
| chr5:149830045 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.466-712_466-703del others(10): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830045 | ||||||
| chr5:149830049 | AAAAAAG | A | 8 | a0002c0002t0005g0059 a0002c0002t0005g0081 a0002c0002t0005g0266 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-712_466-707del others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830049 | ||||||
| chr5:149830050 | AAAAAG | A | 47 | a0001c0004t0018g0034 a0001c0004t0018g0039 a0001c0004t0018g0166 others(44): Show |
47 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.466-712_466-708del others(5): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830050 | ||||||
| chr5:149830055 | G | A | 59 | a0001c0004t0006g0095 a0001c0017t0017g0014 a0002c0002t0005g0016 others(56): Show |
59 | HG00140.hp2 HG00609.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.466-712G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830055 | |||||||
| chr5:149830055 | GA | G | 27 | a0001c0001t0001g0098 a0001c0001t0040g0065 a0001c0004t0006g0102 others(24): Show |
27 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.466-697delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830055 | ||||||
| chr5:149830056 | A | AG | 19 | a0001c0004t0006g0095 a0002c0002t0005g0084 a0002c0002t0005g0168 others(16): Show |
19 | HG00609.hp2 HG01993.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.466-711_466-710ins others(1): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830056 | |||||||
| chr5:149830056 | A | G | 59 | a0001c0004t0006g0193 a0001c0004t0018g0031 a0001c0004t0018g0034 others(56): Show |
59 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.466-711A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830056 | |||||||
| chr5:149830057 | A | AAG | 7 | a0001c0017t0017g0014 a0003c0003t0004g0247 a0003c0003t0004g0305 others(4): Show |
7 | HG01934.hp1 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-709_466-708ins others(2): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830057 | ||||||
| chr5:149830057 | A | AG | 21 | a0003c0003t0004g0150 a0003c0003t0004g0177 a0003c0003t0004g0281 others(18): Show |
21 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.466-710_466-709ins others(1): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830057 | |||||||
| chr5:149830057 | A | G | 1 | a0002c0002t0068g0250 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.466-710A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830057 | |||||||
| chr5:149830058 | A | G | 1 | a0003c0003t0004g0045 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.466-709A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830058 | |||||||
| chr5:149830068 | A | C | 5 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 others(2): Show |
5 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-699A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830068 | |||||||
| chr5:149830203 | C | G | 7 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-564C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830203 | |||||||
| chr5:149830246 | CT | C | 9 | a0001c0001t0051g0145 a0001c0009t0064g0261 a0001c0018t0058g0211 others(6): Show |
9 | HG01074.hp2 HG01943.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.466-509delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 149830246 | ||||||
| chr5:149830261 | T | C | 11 | a0001c0001t0045g0198 a0001c0018t0029g0197 a0001c0018t0029g0217 others(8): Show |
11 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.466-506T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830261 | |||||||
| chr5:149830452 | A | T | 1 | a0001c0001t0003g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.466-315A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830452 | |||||||
| chr5:149830667 | C | T | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-100C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830667 | |||||||
| chr5:149830745 | G | A | 1 | a0001c0004t0062g0252 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.466-22G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 3/11 | chr5 | 149830745 | |||||||
| chr5:149830926 | G | A | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.582+43G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149830926 | |||||||
| chr5:149831023 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.582+140G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831023 | |||||||
| chr5:149831027 | C | T | 5 | a0001c0030t0031g0320 a0008c0016t0026g0009 a0008c0016t0026g0262 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+144C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831027 | |||||||
| chr5:149831285 | C | T | 147 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(144): Show |
147 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.582+402C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831285 | |||||||
| chr5:149831550 | C | T | 1 | a0001c0030t0031g0320 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.582+667C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831550 | |||||||
| chr5:149831640 | A | G | 11 | a0001c0001t0045g0198 a0001c0018t0029g0197 a0001c0018t0029g0217 others(8): Show |
11 | HG00280.hp1 HG01074.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+757A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831640 | |||||||
| chr5:149831730 | C | G | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.582+847C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831730 | |||||||
| chr5:149831754 | G | C | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.582+871G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831754 | |||||||
| chr5:149831755 | G | A | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.582+872G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831755 | |||||||
| chr5:149831781 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.583-875G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831781 | |||||||
| chr5:149831829 | C | G | 33 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(30): Show |
33 | HG00639.hp2 HG01106.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.583-827C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831829 | |||||||
| chr5:149831842 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.583-814A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149831842 | |||||||
| chr5:149832032 | C | T | 1 | a0001c0001t0003g0057 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.583-624C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149832032 | |||||||
| chr5:149832066 | G | A | 1 | a0002c0002t0068g0250 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.583-590G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149832066 | |||||||
| chr5:149832093 | G | A | 1 | a0007c0023t0017g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.583-563G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149832093 | |||||||
| chr5:149832255 | G | A | 10 | a0004c0005t0013g0071 a0004c0005t0013g0236 a0004c0005t0013g0239 others(7): Show |
10 | HG02165.hp2 HG02300.hp2 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.583-401G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149832255 | |||||||
| chr5:149832305 | G | A | 156 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(153): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.583-351G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149832305 | |||||||
| chr5:149832381 | G | A | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.583-275G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149832381 | |||||||
| chr5:149832383 | G | C | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.583-273G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149832383 | |||||||
| chr5:149832390 | T | C | 1 | a0001c0001t0003g0167 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.583-266T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 4/11 | chr5 | 149832390 | |||||||
| chr5:149833893 | A | G | 115 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(112): Show |
115 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.1705+115A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/11 | chr5 | 149833893 | |||||||
| chr5:149834040 | A | G | 2 | a0001c0004t0018g0034 a0001c0004t0018g0039 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1705+262A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/11 | chr5 | 149834040 | |||||||
| chr5:149834132 | T | C | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1705+354T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/11 | chr5 | 149834132 | |||||||
| chr5:149834178 | G | A | 1 | a0001c0001t0053g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1705+400G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/11 | chr5 | 149834178 | |||||||
| chr5:149834181 | G | A | 46 | a0001c0030t0031g0320 a0002c0002t0005g0006 a0002c0002t0005g0016 others(43): Show |
46 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1705+403G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/11 | chr5 | 149834181 | |||||||
| chr5:149834333 | A | T | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1706-341A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/11 | chr5 | 149834333 | |||||||
| chr5:149834604 | C | T | 31 | a0001c0001t0001g0047 a0002c0002t0005g0016 a0002c0002t0005g0059 others(28): Show |
31 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1706-70C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 5/11 | chr5 | 149834604 | |||||||
| chr5:149834744 | A | G | 2 | a0001c0010t0038g0185 a0001c0010t0056g0153 |
2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1742+34A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 6/11 | chr5 | 149834744 | |||||||
| chr5:149834814 | C | T | 52 | a0001c0009t0064g0261 a0001c0030t0031g0320 a0002c0002t0005g0006 others(49): Show |
52 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1742+104C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 6/11 | chr5 | 149834814 | |||||||
| chr5:149835024 | G | A | 49 | a0001c0001t0001g0018 a0001c0001t0001g0149 a0001c0030t0031g0320 others(46): Show |
49 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1743-277G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 6/11 | chr5 | 149835024 | |||||||
| chr5:149835138 | C | T | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1743-163C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 6/11 | chr5 | 149835138 | |||||||
| chr5:149835373 | A | G | 4 | a0001c0017t0017g0014 a0007c0019t0017g0314 a0007c0019t0017g0315 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG03225.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1807+8A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835373 | |||||||
| chr5:149835448 | T | G | 1 | a0003c0003t0011g0301 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1807+83T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835448 | |||||||
| chr5:149835453 | C | T | 1 | a0001c0017t0017g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1807+88C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835453 | |||||||
| chr5:149835467 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1807+102C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835467 | |||||||
| chr5:149835602 | A | G | 2 | a0001c0001t0002g0154 a0001c0001t0002g0173 |
2 | NA19084.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1807+237A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835602 | |||||||
| chr5:149835650 | C | G | 122 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(119): Show |
122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1807+285C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835650 | |||||||
| chr5:149835905 | G | T | 44 | a0002c0002t0005g0006 a0002c0002t0005g0016 a0002c0002t0005g0028 others(41): Show |
44 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1808-358G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835905 | |||||||
| chr5:149835947 | CT | C | 44 | a0002c0002t0005g0006 a0002c0002t0005g0016 a0002c0002t0005g0028 others(41): Show |
44 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1808-306delT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 149835947 | ||||||
| chr5:149835957 | T | C | 1 | a0002c0002t0005g0266 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1808-306T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835957 | |||||||
| chr5:149835958 | C | CT | 49 | a0001c0001t0001g0098 a0001c0001t0001g0165 a0001c0001t0001g0181 others(46): Show |
49 | HG00280.hp1 HG00639.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1808-288dupT | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 149835958 | ||||||
| chr5:149835959 | T | C | 44 | a0002c0002t0005g0006 a0002c0002t0005g0016 a0002c0002t0005g0028 others(41): Show |
44 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1808-304T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149835959 | |||||||
| chr5:149836020 | C | T | 1 | a0001c0004t0006g0193 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1808-243C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149836020 | |||||||
| chr5:149836089 | G | A | 46 | a0001c0030t0031g0320 a0002c0002t0005g0006 a0002c0002t0005g0016 others(43): Show |
46 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.1808-174G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149836089 | |||||||
| chr5:149836149 | A | C | 2 | a0001c0010t0038g0185 a0001c0010t0056g0153 |
2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1808-114A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 7/11 | chr5 | 149836149 | |||||||
| chr5:149837103 | C | T | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2618+30C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837103 | |||||||
| chr5:149837268 | A | T | 2 | a0001c0001t0023g0229 a0001c0001t0041g0222 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2618+195A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837268 | |||||||
| chr5:149837336 | A | C | 1 | a0006c0007t0016g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2618+263A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837336 | |||||||
| chr5:149837424 | A | G | 87 | a0001c0009t0064g0261 a0001c0018t0029g0197 a0001c0018t0029g0217 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.2618+351A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837424 | |||||||
| chr5:149837446 | C | T | 1 | a0001c0001t0007g0187 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2618+373C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837446 | |||||||
| chr5:149837475 | A | G | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2618+402A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837475 | |||||||
| chr5:149837515 | T | C | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2618+442T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837515 | |||||||
| chr5:149837643 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2618+570G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837643 | |||||||
| chr5:149837811 | C | G | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2618+738C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837811 | |||||||
| chr5:149837883 | G | C | 1 | a0002c0002t0005g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2618+810G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837883 | |||||||
| chr5:149837919 | G | A | 30 | a0002c0002t0005g0016 a0002c0002t0005g0059 a0002c0002t0005g0081 others(27): Show |
30 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.2618+846G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149837919 | |||||||
| chr5:149838112 | CA | C | 6 | a0006c0007t0016g0012 a0006c0007t0016g0040 a0006c0007t0016g0131 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2618+1048delA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr5 | 149838112 | ||||||
| chr5:149838122 | T | C | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2618+1049T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149838122 | |||||||
| chr5:149838414 | G | T | 4 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2618+1341G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149838414 | |||||||
| chr5:149838420 | CCT | C | 25 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(22): Show |
25 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.2618+1352_2618+135 others(6): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr5 | 149838420 | ||||||
| chr5:149838447 | G | A | 44 | a0002c0002t0005g0006 a0002c0002t0005g0016 a0002c0002t0005g0028 others(41): Show |
44 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.2618+1374G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149838447 | |||||||
| chr5:149838476 | A | G | 1 | a0001c0001t0053g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2618+1403A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149838476 | |||||||
| chr5:149838627 | G | C | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2619-1414G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149838627 | |||||||
| chr5:149838631 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2619-1410G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149838631 | |||||||
| chr5:149838692 | A | G | 44 | a0002c0002t0005g0006 a0002c0002t0005g0016 a0002c0002t0005g0028 others(41): Show |
44 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.2619-1349A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149838692 | |||||||
| chr5:149838785 | T | C | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2619-1256T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149838785 | |||||||
| chr5:149839323 | C | A | 121 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(118): Show |
121 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2619-718C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149839323 | |||||||
| chr5:149839519 | G | C | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2619-522G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149839519 | |||||||
| chr5:149839757 | G | C | 3 | a0001c0004t0006g0112 a0001c0004t0006g0115 a0001c0004t0030g0113 |
3 | HG00280.hp2 HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2619-284G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149839757 | |||||||
| chr5:149839837 | A | G | 1 | a0002c0002t0065g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2619-204A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149839837 | |||||||
| chr5:149839966 | C | T | 1 | a0004c0005t0001g0121 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2619-75C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 8/11 | chr5 | 149839966 | |||||||
| chr5:149840274 | T | C | 2 | a0001c0001t0003g0151 a0001c0001t0003g0170 |
2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2694+158T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149840274 | |||||||
| chr5:149840350 | C | G | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2694+234C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149840350 | |||||||
| chr5:149840391 | G | A | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2694+275G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149840391 | |||||||
| chr5:149840420 | GGGCTGTG others(19): Show |
G | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2694+310_2694+335d others(28): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr5 | 149840420 | ||||||
| chr5:149840451 | G | A | 7 | a0006c0007t0016g0012 a0006c0007t0016g0035 a0006c0007t0016g0040 others(4): Show |
7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2694+335G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149840451 | |||||||
| chr5:149840541 | A | G | 1 | a0003c0003t0004g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2694+425A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149840541 | |||||||
| chr5:149840542 | C | T | 2 | a0001c0001t0003g0103 a0001c0030t0031g0320 |
2 | HG00544.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2694+426C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149840542 | |||||||
| chr5:149841114 | A | G | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2694+998A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841114 | |||||||
| chr5:149841132 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2694+1016T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841132 | |||||||
| chr5:149841339 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2695-917G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841339 | |||||||
| chr5:149841354 | T | A | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2695-902T>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841354 | |||||||
| chr5:149841474 | C | A | 50 | a0001c0030t0031g0320 a0002c0002t0005g0006 a0002c0002t0005g0016 others(47): Show |
50 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.2695-782C>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841474 | |||||||
| chr5:149841602 | G | A | 14 | a0004c0005t0001g0246 a0004c0005t0001g0248 a0004c0005t0001g0257 others(11): Show |
14 | HG00639.hp2 HG01934.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.2695-654G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841602 | |||||||
| chr5:149841671 | A | T | 21 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(18): Show |
21 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.2695-585A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841671 | |||||||
| chr5:149841851 | T | G | 1 | a0004c0005t0013g0071 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2695-405T>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841851 | |||||||
| chr5:149841932 | G | C | 1 | a0014c0025t0031g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2695-324G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149841932 | |||||||
| chr5:149842131 | G | A | 7 | a0006c0007t0016g0012 a0006c0007t0016g0035 a0006c0007t0016g0040 others(4): Show |
7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2695-125G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149842131 | |||||||
| chr5:149842139 | T | C | 45 | a0001c0009t0064g0261 a0002c0002t0005g0006 a0002c0002t0005g0016 others(42): Show |
45 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.2695-117T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149842139 | |||||||
| chr5:149842205 | C | T | 7 | a0001c0004t0018g0031 a0001c0004t0018g0034 a0001c0004t0018g0039 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2695-51C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149842205 | |||||||
| chr5:149842225 | G | C | 115 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(112): Show |
115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2695-31G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 9/11 | chr5 | 149842225 | |||||||
| chr5:149842388 | C | T | 4 | a0001c0010t0001g0056 a0001c0010t0001g0255 a0001c0010t0001g0256 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2816+11C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842388 | |||||||
| chr5:149842429 | C | T | 28 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(25): Show |
28 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.2816+52C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842429 | |||||||
| chr5:149842444 | G | T | 2 | a0008c0016t0026g0009 a0008c0016t0026g0262 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2816+67G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842444 | |||||||
| chr5:149842470 | G | A | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2816+93G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842470 | |||||||
| chr5:149842592 | C | T | 44 | a0002c0002t0005g0006 a0002c0002t0005g0016 a0002c0002t0005g0028 others(41): Show |
44 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.2816+215C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842592 | |||||||
| chr5:149842594 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2816+217G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842594 | |||||||
| chr5:149842651 | G | A | 2 | a0002c0002t0010g0066 a0002c0002t0010g0304 |
2 | HG01261.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2816+274G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842651 | |||||||
| chr5:149842660 | A | G | 6 | a0006c0007t0016g0012 a0006c0007t0016g0040 a0006c0007t0016g0131 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2816+283A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842660 | |||||||
| chr5:149842806 | A | G | 1 | a0001c0009t0027g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2816+429A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149842806 | |||||||
| chr5:149843124 | C | T | 9 | a0003c0003t0004g0247 a0003c0003t0004g0305 a0003c0003t0011g0063 others(6): Show |
9 | HG01928.hp2 HG01952.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.2816+747C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843124 | |||||||
| chr5:149843184 | G | T | 2 | a0002c0008t0008g0191 a0002c0008t0063g0169 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2816+807G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843184 | |||||||
| chr5:149843185 | T | C | 30 | a0002c0002t0005g0016 a0002c0002t0005g0059 a0002c0002t0005g0081 others(27): Show |
30 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.2816+808T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843185 | |||||||
| chr5:149843379 | C | T | 21 | a0001c0004t0006g0095 a0001c0004t0006g0101 a0001c0004t0006g0102 others(18): Show |
21 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.2816+1002C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843379 | |||||||
| chr5:149843439 | G | A | 29 | a0002c0002t0005g0016 a0002c0002t0005g0059 a0002c0002t0005g0081 others(26): Show |
29 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.2816+1062G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843439 | |||||||
| chr5:149843528 | T | C | 9 | a0003c0003t0004g0287 a0003c0003t0004g0288 a0003c0003t0004g0293 others(6): Show |
9 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.2816+1151T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843528 | |||||||
| chr5:149843614 | C | T | 1 | a0001c0001t0054g0223 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2816+1237C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843614 | |||||||
| chr5:149843641 | G | T | 34 | a0001c0001t0003g0020 a0001c0001t0003g0022 a0001c0001t0003g0024 others(31): Show |
34 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.2816+1264G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843641 | |||||||
| chr5:149843705 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2816+1328G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843705 | |||||||
| chr5:149843839 | G | T | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2816+1462G>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149843839 | |||||||
| chr5:149844125 | T | C | 3 | a0004c0005t0001g0139 a0004c0005t0001g0245 a0004c0005t0012g0249 |
3 | HG01106.hp2 HG01258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2817-1635T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149844125 | |||||||
| chr5:149844466 | C | T | 2 | a0002c0002t0010g0066 a0002c0002t0010g0304 |
2 | HG01261.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2817-1294C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149844466 | |||||||
| chr5:149844467 | G | A | 7 | a0006c0007t0016g0012 a0006c0007t0016g0035 a0006c0007t0016g0040 others(4): Show |
7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2817-1293G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149844467 | |||||||
| chr5:149844767 | T | C | 7 | a0006c0007t0016g0012 a0006c0007t0016g0035 a0006c0007t0016g0040 others(4): Show |
7 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2817-993T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149844767 | |||||||
| chr5:149844894 | A | C | 2 | a0001c0004t0006g0210 a0001c0022t0006g0097 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2817-866A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149844894 | |||||||
| chr5:149845538 | G | C | 1 | a0005c0026t0034g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2817-222G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149845538 | |||||||
| chr5:149845561 | G | A | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2817-199G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149845561 | |||||||
| chr5:149845569 | A | C | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2817-191A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149845569 | |||||||
| chr5:149845747 | T | C | 1 | a0003c0003t0004g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2817-13T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149845747 | |||||||
| chr5:149845748 | C | T | 1 | a0001c0001t0045g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2817-12C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 10/11 | chr5 | 149845748 | |||||||
| chr5:149846038 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2971+124T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846038 | |||||||
| chr5:149846063 | A | C | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2971+149A>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846063 | |||||||
| chr5:149846180 | T | C | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2971+266T>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846180 | |||||||
| chr5:149846255 | C | T | 3 | a0001c0018t0029g0197 a0001c0018t0029g0217 a0001c0018t0058g0211 |
3 | HG00280.hp1 HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2971+341C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846255 | |||||||
| chr5:149846369 | C | T | 1 | a0001c0006t0001g0099 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2971+455C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846369 | |||||||
| chr5:149846507 | G | A | 1 | a0003c0003t0004g0294 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2971+593G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846507 | |||||||
| chr5:149846617 | G | C | 1 | a0002c0002t0065g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2971+703G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846617 | |||||||
| chr5:149846643 | G | GA | 256 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.2971+742dupA | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 149846643 | ||||||
| chr5:149846643 | G | GAA | 21 | a0001c0009t0064g0261 a0001c0017t0006g0219 a0002c0002t0005g0006 others(18): Show |
21 | HG02145.hp1 HG02148.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2971+741_2971+742d others(4): Show |
PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 149846643 | ||||||
| chr5:149846735 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2972-723C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846735 | |||||||
| chr5:149846738 | C | G | 4 | a0002c0002t0005g0084 a0002c0002t0005g0168 a0002c0002t0032g0041 others(1): Show |
4 | NA18941.hp2 NA18994.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2972-720C>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846738 | |||||||
| chr5:149846852 | C | T | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2972-606C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846852 | |||||||
| chr5:149846956 | A | G | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2972-502A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846956 | |||||||
| chr5:149846958 | A | T | 1 | a0010c0021t0061g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2972-500A>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149846958 | |||||||
| chr5:149847004 | G | C | 4 | a0002c0014t0005g0017 a0002c0014t0005g0019 a0002c0014t0005g0259 others(1): Show |
4 | HG00609.hp2 HG02165.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2972-454G>C | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149847004 | |||||||
| chr5:149847070 | G | A | 30 | a0003c0003t0004g0045 a0003c0003t0004g0150 a0003c0003t0004g0177 others(27): Show |
30 | HG00140.hp2 HG01433.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2972-388G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149847070 | |||||||
| chr5:149847198 | A | G | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2972-260A>G | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149847198 | |||||||
| chr5:149847365 | G | A | 1 | a0001c0001t0007g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2972-93G>A | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149847365 | |||||||
| chr5:149847386 | C | T | 4 | a0008c0016t0026g0009 a0008c0016t0026g0262 a0008c0016t0036g0122 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2972-72C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149847386 | |||||||
| chr5:149847429 | C | T | 2 | a0001c0001t0002g0278 a0001c0001t0002g0307 |
2 | HG00738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2972-29C>T | PPARGC1B | ENSG00000155846.17 | transcript | ENST00000309241.10 | protein_coding | 11/11 | chr5 | 149847429 |