Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2735 |
| ensemblid | ENSG00000111087.10 |
| hgncid | 4317 |
| symbol | GLI1 |
| name | GLI family zinc finger 1 |
| refseq_nuc | NM_005269.3 |
| refseq_prot | NP_005260.1 |
| ensembl_nuc | ENST00000228682.7 |
| ensembl_prot | ENSP00000228682.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 57459785 |
| end | 57472268 |
| strand | + |
| ver | v1.2 |
| region | chr12:57459785-57472268 |
| region5000 | chr12:57454785-57477268 |
| regionname0 | GLI1_chr12_57459785_57472268 |
| regionname5000 | GLI1_chr12_57454785_57477268 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1106 | 170 | 26 | 34 | 86 | 4 | 19 | 64 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0002 | 0/1 | 1106 | 153 | 19 | 30 | 86 | 5 | 12 | 69 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0003 | 0/0 | 1106 | 61 | 52 | 5 | 0 | 0 | 4 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0004 | 0/0 | 1106 | 17 | 0 | 0 | 16 | 0 | 1 | 8 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0005 | 0/0 | 1106 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0006 | 0/0 | 1106 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0007 | 0/0 | 1106 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0008 | 0/0 | 188 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(183): Show |
chr12 | 57454785 | 57477268 |
| a0009 | 0/0 | 1106 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0010 | 0/0 | 1106 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0011 | 0/0 | 1106 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0012 | 0/0 | 1106 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0013 | 0/0 | 1106 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0014 | 0/0 | 1106 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0015 | 0/0 | 1106 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| a0016 | 0/0 | 1106 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | MFNSM others(1101): Show |
chr12 | 57454785 | 57477268 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3318 | 167 | 25 | 33 | 85 | 4 | 19 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0001c0009 | 0/0 | 3318 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0001c0011 | 0/0 | 3318 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0001c0014 | 0/0 | 3318 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0002c0002 | 0/1 | 3318 | 150 | 17 | 30 | 85 | 5 | 12 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0002c0012 | 0/0 | 3318 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0002c0013 | 0/0 | 3318 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0002c0017 | 0/0 | 3318 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0003c0003 | 0/0 | 3318 | 37 | 33 | 3 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0003c0004 | 0/0 | 3318 | 18 | 15 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0003c0006 | 0/0 | 3318 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0003c0007 | 0/0 | 3318 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0004c0005 | 0/0 | 3318 | 16 | 0 | 0 | 15 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0004c0016 | 0/0 | 3318 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0005c0008 | 0/0 | 3318 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0006c0020 | 0/0 | 3318 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0007c0018 | 0/0 | 3318 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0008c0022 | 0/0 | 3347 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3342): Show |
chr12 | 57454785 | 57477268 | ||
| a0009c0015 | 0/0 | 3318 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0010c0021 | 0/0 | 3318 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0011c0023 | 0/0 | 3318 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0012c0010 | 0/0 | 3318 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0013c0025 | 0/0 | 3318 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0014c0024 | 0/0 | 3318 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0015c0026 | 0/0 | 3318 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 | ||
| a0016c0019 | 0/0 | 3318 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | ATGTT others(3313): Show |
chr12 | 57454785 | 57477268 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3972 | 154 | 19 | 32 | 81 | 4 | 18 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0001t0002 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0001t0003 | 1/0 | 3972 | 7 | 5 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0001t0007 | 0/0 | 3972 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0001t0011 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0001t0012 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0001t0015 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0009t0001 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0011t0001 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0001c0014t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0001 | 0/1 | 3972 | 138 | 14 | 28 | 80 | 5 | 10 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0002 | 0/0 | 3972 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0004 | 0/0 | 3972 | 2 | 0 | 2 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0006 | 0/0 | 3972 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0008 | 0/0 | 3972 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | TTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0009 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0010 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0013 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0002t0014 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0012t0001 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0013t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0002c0017t0001 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0003c0003t0001 | 0/0 | 3972 | 36 | 33 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0003c0003t0016 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0003c0004t0001 | 0/0 | 3972 | 16 | 13 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0003c0004t0005 | 0/0 | 3972 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0003c0006t0001 | 0/0 | 3972 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0003c0007t0001 | 0/0 | 3972 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0004c0005t0002 | 0/0 | 3972 | 16 | 0 | 0 | 15 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0004c0016t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0005c0008t0001 | 0/0 | 3972 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0006c0020t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0007c0018t0001 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0008c0022t0001 | 0/0 | 4001 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3996): Show |
chr12 | 57454785 | 57477268 |
| a0009c0015t0001 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0010c0021t0001 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0011c0023t0001 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0012c0010t0001 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0013c0025t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0014c0024t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0015c0026t0001 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| a0016c0019t0001 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | GTAAG others(3967): Show |
chr12 | 57454785 | 57477268 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 92 | 11 | 20 | 45 | 2 | 14 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0003 | 0/0 | 16 | 1 | 2 | 13 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0006 | 0/0 | 12 | 0 | 5 | 7 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0012 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0003g0001 | 1/0 | 7 | 5 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0011t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0001c0014t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0002 | 0/1 | 93 | 4 | 23 | 51 | 5 | 9 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0008g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0012t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0013t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0002c0017t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0008 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0003t0016g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0004t0001g0005 | 0/0 | 11 | 8 | 2 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0004t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0004t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0006t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0003c0007t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0004c0005t0002g0007 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0004c0005t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0004c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0004c0016t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0005c0008t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0006c0020t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0007c0018t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0008c0022t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0009c0015t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0010c0021t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0011c0023t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0012c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0013c0025t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0014c0024t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0015c0026t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| a0016c0019t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00544 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00544 | hp2 | a0004 | c0016 | t0001 | g0014 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00673 | hp2 | a0006 | c0020 | t0001 | g0019 | EAS | CHS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00738 | hp2 | a0007 | c0018 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0036 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01175 | hp1 | a0002 | c0002 | t0004 | g0072 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01192 | hp1 | a0001 | c0009 | t0001 | g0001 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01243 | hp2 | a0003 | c0003 | t0016 | g0008 | AMR | PUR | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01255 | hp1 | a0003 | c0004 | t0001 | g0005 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01257 | hp1 | a0002 | c0002 | t0004 | g0073 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01261 | hp1 | a0003 | c0004 | t0001 | g0005 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01515 | hp1 | a0008 | c0022 | t0001 | g0065 | EUR | IBS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01891 | hp1 | a0002 | c0012 | t0001 | g0015 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0033 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01928 | hp1 | a0009 | c0015 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01978 | hp1 | a0010 | c0021 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02015 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02027 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0061 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02055 | hp2 | a0003 | c0004 | t0001 | g0034 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02071 | hp2 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02129 | hp2 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02165 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | CDX | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02257 | hp1 | a0005 | c0008 | t0001 | g0026 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0010 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02451 | hp1 | a0003 | c0006 | t0001 | g0013 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02523 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0049 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02630 | hp2 | a0002 | c0002 | t0006 | g0002 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0021 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02683 | hp1 | a0011 | c0023 | t0001 | g0046 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02698 | hp1 | a0003 | c0007 | t0001 | g0030 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02723 | hp1 | a0002 | c0002 | t0006 | g0002 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02809 | hp1 | a0003 | c0006 | t0001 | g0013 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02809 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0031 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02818 | hp2 | a0003 | c0006 | t0001 | g0013 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02886 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0053 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0021 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0050 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02970 | hp1 | a0005 | c0008 | t0001 | g0026 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02970 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02976 | hp1 | a0003 | c0004 | t0005 | g0005 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03041 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03041 | hp2 | a0003 | c0006 | t0001 | g0013 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0082 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0083 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03130 | hp2 | a0001 | c0011 | t0001 | g0041 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03195 | hp1 | a0003 | c0004 | t0001 | g0021 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03195 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03239 | hp1 | a0003 | c0004 | t0001 | g0005 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0078 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03486 | hp1 | a0003 | c0004 | t0005 | g0005 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03490 | hp2 | a0002 | c0002 | t0008 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03492 | hp2 | a0002 | c0002 | t0008 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0010 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03704 | hp2 | a0012 | c0010 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03834 | hp1 | a0003 | c0007 | t0001 | g0030 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03927 | hp1 | a0004 | c0005 | t0002 | g0007 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG04115 | hp2 | a0001 | c0001 | t0015 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0079 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18948 | hp1 | a0002 | c0013 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18960 | hp2 | a0004 | c0005 | t0002 | g0007 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18967 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18978 | hp1 | a0002 | c0002 | t0013 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18979 | hp1 | a0004 | c0005 | t0002 | g0007 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18980 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18984 | hp1 | a0013 | c0025 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19003 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19006 | hp1 | a0002 | c0002 | t0009 | g0040 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19011 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19030 | hp1 | a0002 | c0002 | t0014 | g0080 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19054 | hp1 | a0002 | c0002 | t0010 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19058 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19060 | hp1 | a0001 | c0014 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19064 | hp2 | a0004 | c0005 | t0002 | g0007 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19068 | hp1 | a0014 | c0024 | t0001 | g0075 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19078 | hp2 | a0015 | c0026 | t0001 | g0035 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19082 | hp1 | a0004 | c0005 | t0002 | g0077 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | YRI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ASW | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02109 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0010 | AFR | MSL | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | USA | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| HG06807 | hp2 | a0002 | c0017 | t0001 | g0069 | AFR | USA | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | USA | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA21309 | hp1 | a0016 | c0019 | t0001 | g0001 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | LWK | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0002 | REF | REF | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0001 | REF | REF | GLI1_chr12_57454785_57477268 | GLI1 | chr12 | 57454785 | 57477268 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57464023 | A | T | 1 | a0015 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.125A>T | p.His42Leu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/12 | 569/3972 | 125/3321 | 42/1106 | chr12 | 57464023 | |||
| chr12:57464730 | C | T | 1 | a0013 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.251C>T | p.Ser84Phe | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/12 | 695/3972 | 251/3321 | 84/1106 | chr12 | 57464730 | |||
| chr12:57464777 | C | G | 1 | a0014 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.298C>G | p.Arg100Gly | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/12 | 742/3972 | 298/3321 | 100/1106 | chr12 | 57464777 | |||
| chr12:57464778 | G | C | 1 | a0014 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.299G>C | p.Arg100Pro | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/12 | 743/3972 | 299/3321 | 100/1106 | chr12 | 57464778 | |||
| chr12:57465224 | C | G | 1 | a0011 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.503C>G | p.Pro168Arg | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 5/12 | 947/3972 | 503/3321 | 168/1106 | chr12 | 57465224 | |||
| chr12:57465242 | T | TGCAACTA others(22): Show |
1 | a0008 | 1 | HG01515.hp1 | frameshift_variant | HIGH | c.521_522insGCAACTAG others(21): Show |
p.Phe174fs | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 5/12 | 966/3972 | 522/3321 | 174/1106 | chr12 | 57465242 | |||
| chr12:57465245 | C | A | 1 | a0008 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.524C>A | p.Pro175Gln | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 5/12 | 968/3972 | 524/3321 | 175/1106 | chr12 | 57465245 | |||
| chr12:57466297 | G | C | 1 | a0009 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.820G>C | p.Gly274Arg | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/12 | 1264/3972 | 820/3321 | 274/1106 | chr12 | 57466297 | |||
| chr12:57468130 | G | A | 1 | a0005 | 2 | HG02257.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.1214G>A | p.Arg405Gln | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/12 | 1658/3972 | 1214/3321 | 405/1106 | chr12 | 57468130 | |||
| chr12:57470361 | C | T | 1 | a0010 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1621C>T | p.Arg541Cys | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2065/3972 | 1621/3321 | 541/1106 | chr12 | 57470361 | |||
| chr12:57470409 | C | T | 1 | a0006 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1669C>T | p.Arg557Cys | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2113/3972 | 1669/3321 | 557/1106 | chr12 | 57470409 | |||
| chr12:57470995 | C | T | 1 | a0016 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.2255C>T | p.Pro752Leu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2699/3972 | 2255/3321 | 752/1106 | chr12 | 57470995 | |||
| chr12:57471063 | C | G | 1 | a0007 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2323C>G | p.Pro775Ala | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2767/3972 | 2323/3321 | 775/1106 | chr12 | 57471063 | |||
| chr12:57471538 | G | A | 6 | a0002 a0011 a0012 others(3): Show |
157 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
missense_variant | MODERATE | c.2798G>A | p.Gly933Asp | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3242/3972 | 2798/3321 | 933/1106 | chr12 | 57471538 | |||
| chr12:57471775 | G | T | 1 | a0004 | 17 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(14): Show |
missense_variant | MODERATE | c.3035G>T | p.Gly1012Val | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3479/3972 | 3035/3321 | 1012/1106 | chr12 | 57471775 | |||
| chr12:57471942 | C | T | 1 | a0012 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.3202C>T | p.Arg1068Trp | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3646/3972 | 3202/3321 | 1068/1106 | chr12 | 57471942 | |||
| chr12:57472038 | G | C | 9 | a0002 a0003 a0004 others(6): Show |
237 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(234): Show |
missense_variant | MODERATE | c.3298G>C | p.Glu1100Gln | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3742/3972 | 3298/3321 | 1100/1106 | chr12 | 57472038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57464770 | G | A | 1 | a0001c0009 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.291G>A | p.Thr97Thr | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/12 | 735/3972 | 291/3321 | 97/1106 | chr12 | 57464770 | |||
| chr12:57465648 | G | A | 9 | a0001c0011 a0002c0002 a0002c0012 others(6): Show |
157 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
synonymous_variant | LOW | c.576G>A | p.Glu192Glu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 6/12 | 1020/3972 | 576/3321 | 192/1106 | chr12 | 57465648 | |||
| chr12:57465829 | G | A | 1 | a0001c0014 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.666G>A | p.Glu222Glu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/12 | 1110/3972 | 666/3321 | 222/1106 | chr12 | 57465829 | |||
| chr12:57466263 | C | T | 1 | a0003c0004 | 18 | HG01255.hp1 HG01261.hp1 HG02055.hp2 others(15): Show |
synonymous_variant | LOW | c.786C>T | p.His262His | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/12 | 1230/3972 | 786/3321 | 262/1106 | chr12 | 57466263 | |||
| chr12:57467356 | C | T | 1 | a0002c0013 | 1 | NA18948.hp1 | synonymous_variant | LOW | c.936C>T | p.Tyr312Tyr | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/12 | 1380/3972 | 936/3321 | 312/1106 | chr12 | 57467356 | |||
| chr12:57468002 | T | C | 1 | a0003c0007 | 2 | HG02698.hp1 HG03834.hp1 |
synonymous_variant | LOW | c.1086T>C | p.Tyr362Tyr | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/12 | 1530/3972 | 1086/3321 | 362/1106 | chr12 | 57468002 | |||
| chr12:57469607 | T | C | 1 | a0004c0016 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1485T>C | p.Leu495Leu | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 11/12 | 1929/3972 | 1485/3321 | 495/1106 | chr12 | 57469607 | |||
| chr12:57469682 | C | T | 1 | a0002c0012 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1560C>T | p.Pro520Pro | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 11/12 | 2004/3972 | 1560/3321 | 520/1106 | chr12 | 57469682 | |||
| chr12:57470876 | C | T | 1 | a0005c0008 | 2 | HG02257.hp1 HG02970.hp1 |
synonymous_variant | LOW | c.2136C>T | p.Ser712Ser | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 2580/3972 | 2136/3321 | 712/1106 | chr12 | 57470876 | |||
| chr12:57472058 | C | T | 1 | a0003c0006 | 4 | HG02451.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
synonymous_variant | LOW | c.3318C>T | p.Ala1106Ala | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 3762/3972 | 3318/3321 | 1106/1106 | chr12 | 57472058 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57459785 | G | T | 1 | a0002c0002t0008 | 2 | HG03490.hp2 HG03492.hp2 |
5_prime_UTR_variant | MODIFIER | c.-444G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3907 | chr12 | 57459785 | ||||||
| chr12:57459816 | G | A | 1 | a0002c0002t0004 | 2 | HG01175.hp1 HG01257.hp1 |
5_prime_UTR_variant | MODIFIER | c.-413G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3876 | chr12 | 57459816 | ||||||
| chr12:57459838 | G | T | 1 | a0003c0003t0016 | 1 | HG01243.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-391G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | chr12 | 57459838 | |||||||
| chr12:57459848 | C | G | 1 | a0001c0001t0015 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-381C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3844 | chr12 | 57459848 | ||||||
| chr12:57459993 | A | G | 1 | a0002c0002t0014 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-236A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3699 | chr12 | 57459993 | ||||||
| chr12:57460025 | C | T | 1 | a0002c0002t0013 | 1 | NA18978.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-204C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | chr12 | 57460025 | |||||||
| chr12:57460083 | T | G | 1 | a0002c0002t0009 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-146T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3609 | chr12 | 57460083 | ||||||
| chr12:57460094 | T | G | 1 | a0003c0004t0005 | 2 | HG02976.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-135T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3598 | chr12 | 57460094 | ||||||
| chr12:57460124 | C | T | 1 | a0001c0001t0012 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3568 | chr12 | 57460124 | ||||||
| chr12:57460125 | C | G | 1 | a0001c0001t0007 | 2 | HG02129.hp1 NA19011.hp2 |
5_prime_UTR_variant | MODIFIER | c.-104C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3567 | chr12 | 57460125 | ||||||
| chr12:57460159 | C | A | 1 | a0002c0002t0010 | 1 | NA19054.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3533 | chr12 | 57460159 | ||||||
| chr12:57460171 | C | G | 3 | a0001c0001t0002 a0002c0002t0002 a0004c0005t0002 |
19 | HG00544.hp1 HG02015.hp1 HG02027.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-58C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/12 | 3521 | chr12 | 57460171 | ||||||
| chr12:57472078 | T | G | 1 | a0002c0002t0006 | 2 | HG02630.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 17 | chr12 | 57472078 | ||||||
| chr12:57472145 | A | C | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(38): Show |
406 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(403): Show |
3_prime_UTR_variant | MODIFIER | c.*84A>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 84 | chr12 | 57472145 | ||||||
| chr12:57472172 | G | A | 1 | a0001c0001t0011 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*111G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 12/12 | 111 | chr12 | 57472172 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57460206 | GA | G | 11 | a0002c0002t0001g0015 a0002c0002t0001g0081 a0002c0002t0014g0080 others(8): Show |
23 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
splice_region_variant&intron_variant | LOW | c.-28+7delA | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 57460206 | ||||||
| chr12:57460208 | A | AG | 8 | a0001c0001t0001g0076 a0001c0001t0002g0074 a0002c0002t0002g0029 others(5): Show |
22 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.-28+14dupG | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 57460208 | ||||||
| chr12:57460302 | A | G | 2 | a0002c0002t0004g0072 a0002c0002t0004g0073 |
2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-28+101A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460302 | |||||||
| chr12:57460338 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-28+137C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460338 | |||||||
| chr12:57460374 | C | T | 1 | a0004c0005t0002g0077 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-28+173C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460374 | |||||||
| chr12:57460500 | T | G | 63 | a0001c0001t0001g0047 a0001c0001t0002g0074 a0001c0011t0001g0041 others(60): Show |
228 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.-28+299T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460500 | |||||||
| chr12:57460528 | G | T | 51 | a0001c0001t0001g0047 a0001c0011t0001g0041 a0002c0002t0001g0002 others(48): Show |
198 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.-28+327G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460528 | |||||||
| chr12:57460542 | A | G | 4 | a0004c0005t0002g0007 a0004c0005t0002g0014 a0004c0005t0002g0077 others(1): Show |
17 | HG00544.hp1 HG00544.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28+341A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460542 | |||||||
| chr12:57460779 | G | C | 1 | a0001c0001t0001g0006 | 12 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28+578G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460779 | |||||||
| chr12:57460863 | G | A | 1 | a0003c0004t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-28+662G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460863 | |||||||
| chr12:57460870 | A | G | 2 | a0003c0003t0001g0013 a0003c0006t0001g0013 |
5 | HG02451.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+669A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460870 | |||||||
| chr12:57460879 | C | T | 1 | a0003c0007t0001g0030 | 2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28+678C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460879 | |||||||
| chr12:57460999 | G | T | 1 | a0003c0007t0001g0030 | 2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28+798G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57460999 | |||||||
| chr12:57461017 | C | G | 1 | a0003c0003t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-28+816C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57461017 | |||||||
| chr12:57461353 | C | A | 1 | a0001c0001t0001g0027 | 2 | HG01106.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-28+1152C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57461353 | |||||||
| chr12:57461397 | G | A | 45 | a0001c0001t0001g0047 a0001c0011t0001g0041 a0002c0002t0001g0002 others(42): Show |
177 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.-28+1196G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57461397 | |||||||
| chr12:57461887 | A | T | 2 | a0001c0001t0001g0070 a0002c0017t0001g0069 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-28+1686A>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57461887 | |||||||
| chr12:57462057 | CAGCTAGG others(18): Show |
C | 1 | a0015c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-1606_-27-1582d others(27): Show |
GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 57462057 | ||||||
| chr12:57462084 | C | G | 7 | a0003c0003t0001g0008 a0003c0003t0001g0048 a0003c0003t0001g0050 others(4): Show |
16 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-27-1581C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462084 | |||||||
| chr12:57462192 | C | A | 1 | a0015c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-1473C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462192 | |||||||
| chr12:57462231 | C | T | 35 | a0001c0001t0001g0047 a0001c0011t0001g0041 a0002c0002t0001g0002 others(32): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.-27-1434C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462231 | |||||||
| chr12:57462252 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-27-1413G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462252 | |||||||
| chr12:57462285 | T | C | 1 | a0003c0003t0001g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-27-1380T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462285 | |||||||
| chr12:57462404 | T | C | 1 | a0002c0002t0001g0037 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-27-1261T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462404 | |||||||
| chr12:57462413 | GCGCCGGC others(10): Show |
G | 1 | a0003c0003t0001g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-27-1248_-27-1232d others(19): Show |
GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 57462413 | ||||||
| chr12:57462434 | T | A | 1 | a0015c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-1231T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462434 | |||||||
| chr12:57462710 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0066 others(2): Show |
20 | HG01358.hp1 HG01952.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.-27-955A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462710 | |||||||
| chr12:57462849 | CACTGCAG others(23): Show |
C | 1 | a0008c0022t0001g0065 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-27-815_-27-786del others(30): Show |
GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462849 | |||||||
| chr12:57462884 | G | C | 34 | a0001c0011t0001g0041 a0002c0002t0001g0002 a0002c0002t0001g0004 others(31): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.-27-781G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462884 | |||||||
| chr12:57462962 | C | T | 1 | a0003c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-27-703C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462962 | |||||||
| chr12:57462993 | C | G | 42 | a0001c0011t0001g0041 a0002c0002t0001g0002 a0002c0002t0001g0004 others(39): Show |
165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-27-672C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57462993 | |||||||
| chr12:57463012 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-27-653G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463012 | |||||||
| chr12:57463150 | C | T | 42 | a0001c0011t0001g0041 a0002c0002t0001g0002 a0002c0002t0001g0004 others(39): Show |
165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-27-515C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463150 | |||||||
| chr12:57463177 | T | G | 1 | a0015c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-488T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463177 | |||||||
| chr12:57463217 | G | A | 36 | a0001c0011t0001g0041 a0002c0002t0001g0002 a0002c0002t0001g0004 others(33): Show |
157 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-27-448G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463217 | |||||||
| chr12:57463335 | AGCCTTCC others(6): Show |
A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-27-329_-27-317del others(13): Show |
GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463335 | |||||||
| chr12:57463517 | G | A | 1 | a0001c0001t0001g0011 | 5 | NA18945.hp1 NA18951.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-148G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463517 | |||||||
| chr12:57463555 | T | A | 1 | a0015c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27-110T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463555 | |||||||
| chr12:57463571 | T | C | 64 | a0001c0011t0001g0041 a0002c0002t0001g0002 a0002c0002t0001g0004 others(61): Show |
232 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.-27-94T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 1/11 | chr12 | 57463571 | |||||||
| chr12:57464228 | C | G | 1 | a0011c0023t0001g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.193+137C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464228 | |||||||
| chr12:57464232 | G | T | 5 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0082 others(2): Show |
16 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+141G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464232 | |||||||
| chr12:57464233 | A | G | 5 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0082 others(2): Show |
16 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+142A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464233 | |||||||
| chr12:57464247 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.193+156G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464247 | |||||||
| chr12:57464265 | T | A | 1 | a0015c0026t0001g0035 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.193+174T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464265 | |||||||
| chr12:57464290 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.193+199G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464290 | |||||||
| chr12:57464305 | T | A | 3 | a0003c0003t0001g0048 a0003c0003t0001g0050 a0005c0008t0001g0026 |
4 | HG02257.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+214T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464305 | |||||||
| chr12:57464489 | T | G | 1 | a0003c0003t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.194-184T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464489 | |||||||
| chr12:57464525 | C | CA | 13 | a0001c0001t0001g0028 a0002c0002t0001g0024 a0002c0002t0004g0072 others(10): Show |
23 | HG01175.hp1 HG01433.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-131dupA | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 57464525 | ||||||
| chr12:57464525 | CA | C | 10 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0002c0002t0001g0020 others(7): Show |
17 | HG00323.hp1 HG01167.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.194-131delA | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr12 | 57464525 | ||||||
| chr12:57464631 | A | G | 37 | a0001c0001t0001g0062 a0001c0011t0001g0041 a0002c0002t0001g0002 others(34): Show |
158 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.194-42A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464631 | |||||||
| chr12:57464638 | T | C | 5 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0082 others(2): Show |
16 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.194-35T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464638 | |||||||
| chr12:57464650 | G | A | 1 | a0002c0002t0001g0038 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.194-23G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464650 | |||||||
| chr12:57464655 | C | T | 1 | a0001c0001t0011g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.194-18C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464655 | |||||||
| chr12:57464656 | G | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0060 a0006c0020t0001g0019 |
5 | HG00673.hp2 NA18941.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-17G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 3/11 | chr12 | 57464656 | |||||||
| chr12:57464894 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.389+26C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/11 | chr12 | 57464894 | |||||||
| chr12:57464950 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.389+82C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/11 | chr12 | 57464950 | |||||||
| chr12:57465047 | A | G | 1 | a0003c0003t0001g0023 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.390-64A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/11 | chr12 | 57465047 | |||||||
| chr12:57465052 | G | A | 36 | a0001c0011t0001g0041 a0002c0002t0001g0002 a0002c0002t0001g0004 others(33): Show |
157 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.390-59G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 4/11 | chr12 | 57465052 | |||||||
| chr12:57465376 | G | T | 1 | a0002c0002t0001g0044 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.534+121G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 5/11 | chr12 | 57465376 | |||||||
| chr12:57465985 | A | G | 1 | a0001c0001t0001g0012 | 5 | HG02280.hp2 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+60A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/11 | chr12 | 57465985 | |||||||
| chr12:57466097 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.763-143T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/11 | chr12 | 57466097 | |||||||
| chr12:57466143 | G | C | 2 | a0002c0002t0001g0022 a0002c0002t0001g0025 |
5 | HG01884.hp2 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.763-97G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/11 | chr12 | 57466143 | |||||||
| chr12:57466149 | G | A | 40 | a0001c0011t0001g0041 a0002c0002t0001g0002 a0002c0002t0001g0004 others(37): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.763-91G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 7/11 | chr12 | 57466149 | |||||||
| chr12:57466593 | T | C | 8 | a0003c0003t0001g0010 a0003c0003t0001g0018 a0003c0003t0001g0023 others(5): Show |
16 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.912+204T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466593 | |||||||
| chr12:57466688 | G | A | 1 | a0002c0002t0001g0039 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.912+299G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466688 | |||||||
| chr12:57466809 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.912+420C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466809 | |||||||
| chr12:57466839 | G | A | 8 | a0003c0003t0001g0016 a0003c0003t0001g0032 a0003c0003t0001g0036 others(5): Show |
24 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.912+450G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466839 | |||||||
| chr12:57466861 | G | A | 1 | a0002c0002t0009g0040 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.912+472G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466861 | |||||||
| chr12:57466882 | C | T | 36 | a0001c0011t0001g0041 a0002c0002t0001g0002 a0002c0002t0001g0004 others(33): Show |
157 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.913-451C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466882 | |||||||
| chr12:57466898 | C | T | 1 | a0005c0008t0001g0026 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.913-435C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466898 | |||||||
| chr12:57466913 | A | T | 9 | a0001c0001t0001g0067 a0003c0003t0001g0016 a0003c0003t0001g0032 others(6): Show |
25 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.913-420A>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466913 | |||||||
| chr12:57466914 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.913-419T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466914 | |||||||
| chr12:57466921 | T | A | 2 | a0003c0003t0001g0016 a0003c0003t0001g0036 |
5 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.913-412T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466921 | |||||||
| chr12:57466922 | A | T | 8 | a0003c0003t0001g0010 a0003c0003t0001g0018 a0003c0003t0001g0023 others(5): Show |
16 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.913-411A>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466922 | |||||||
| chr12:57466945 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.913-388G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57466945 | |||||||
| chr12:57467008 | C | A | 2 | a0002c0002t0004g0072 a0002c0002t0004g0073 |
2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.913-325C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467008 | |||||||
| chr12:57467027 | G | A | 2 | a0002c0002t0004g0072 a0002c0002t0004g0073 |
2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.913-306G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467027 | |||||||
| chr12:57467030 | C | T | 1 | a0003c0003t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.913-303C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467030 | |||||||
| chr12:57467043 | T | C | 60 | a0001c0001t0001g0062 a0001c0011t0001g0041 a0002c0002t0001g0002 others(57): Show |
219 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.913-290T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467043 | |||||||
| chr12:57467088 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.913-245G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467088 | |||||||
| chr12:57467124 | T | C | 1 | a0002c0002t0004g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.913-209T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467124 | |||||||
| chr12:57467126 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-207T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467126 | |||||||
| chr12:57467130 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-203C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467130 | |||||||
| chr12:57467131 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-202A>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467131 | |||||||
| chr12:57467134 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-199G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467134 | |||||||
| chr12:57467140 | G | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-193G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467140 | |||||||
| chr12:57467142 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-191G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467142 | |||||||
| chr12:57467152 | G | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-181G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467152 | |||||||
| chr12:57467156 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-177C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467156 | |||||||
| chr12:57467159 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-174T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467159 | |||||||
| chr12:57467170 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-163C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467170 | |||||||
| chr12:57467172 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-161T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467172 | |||||||
| chr12:57467173 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-160G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467173 | |||||||
| chr12:57467177 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-156G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467177 | |||||||
| chr12:57467178 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-155C>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467178 | |||||||
| chr12:57467179 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-154C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467179 | |||||||
| chr12:57467189 | T | C | 8 | a0003c0003t0001g0016 a0003c0003t0001g0032 a0003c0003t0001g0036 others(5): Show |
24 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.913-144T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467189 | |||||||
| chr12:57467192 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-141T>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467192 | |||||||
| chr12:57467198 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-135G>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467198 | |||||||
| chr12:57467199 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-134A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467199 | |||||||
| chr12:57467200 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-133A>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467200 | |||||||
| chr12:57467207 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-126C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467207 | |||||||
| chr12:57467214 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-119C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467214 | |||||||
| chr12:57467227 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-106T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467227 | |||||||
| chr12:57467228 | C | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-105C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467228 | |||||||
| chr12:57467234 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-99T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467234 | |||||||
| chr12:57467236 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-97A>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467236 | |||||||
| chr12:57467237 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-96T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467237 | |||||||
| chr12:57467238 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913-95A>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 8/11 | chr12 | 57467238 | |||||||
| chr12:57467536 | G | C | 2 | a0004c0005t0002g0007 a0004c0005t0002g0077 |
12 | HG00544.hp1 HG02015.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1077+39G>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467536 | |||||||
| chr12:57467558 | C | T | 1 | a0002c0002t0002g0029 | 2 | NA18971.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1077+61C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467558 | |||||||
| chr12:57467621 | C | T | 1 | a0002c0002t0001g0017 | 4 | NA18944.hp1 NA18960.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+124C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467621 | |||||||
| chr12:57467701 | A | G | 62 | a0001c0001t0001g0062 a0002c0002t0001g0002 a0002c0002t0001g0004 others(59): Show |
232 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1077+204A>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467701 | |||||||
| chr12:57467875 | C | A | 1 | a0003c0003t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1078-119C>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 9/11 | chr12 | 57467875 | |||||||
| chr12:57468443 | C | T | 1 | a0003c0004t0001g0021 | 3 | HG02647.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1308+219C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57468443 | |||||||
| chr12:57468823 | C | T | 7 | a0003c0003t0001g0010 a0003c0003t0001g0018 a0003c0003t0001g0031 others(4): Show |
14 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1308+599C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57468823 | |||||||
| chr12:57469134 | T | G | 10 | a0003c0003t0001g0013 a0003c0003t0001g0016 a0003c0003t0001g0032 others(7): Show |
29 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1309-297T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469134 | |||||||
| chr12:57469171 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1309-260C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469171 | |||||||
| chr12:57469233 | T | C | 1 | a0002c0002t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1309-198T>C | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469233 | |||||||
| chr12:57469293 | T | G | 1 | a0002c0002t0001g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1309-138T>G | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469293 | |||||||
| chr12:57469353 | G | A | 1 | a0002c0002t0001g0043 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1309-78G>A | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 10/11 | chr12 | 57469353 | |||||||
| chr12:57470015 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1577-302C>T | GLI1 | ENSG00000111087.10 | transcript | ENST00000228682.7 | protein_coding | 11/11 | chr12 | 57470015 |