| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74872935-74873109 | Rare:38 | ||||
| chr15:74873215-74873488 | Common:6; Rare:78 | ||||
| chr15:74889738-74890076 | Rare:92; Clinvar (pathogenic):1 | ||||
| chr15:74906789-74906881 | Rare:42 | ||||
| chr15:74937976-74938265 | Common:2; Rare:97 | ||||
| chr15:74995363-74995636 | Common:7; Rare:105 | ||||
| chr15:75335973-75336091 | Common:1; Rare:53 | ||||
| chr15:75347481-75347910 | Common:2; Rare:112 | ||||
| chr15:75348173-75348272 | Common:1; Rare:27 | ||||
| chr15:75362018-75362332 | Common:4; Rare:66 | ||||
| chr15:75367979-75368155 | Rare:78 | ||||
| chr15:75368519-75368810 | Rare:96 | ||||
| chr15:75451668-75451988 | Common:1; Rare:88 | ||||
| chr15:75455744-75455952 | Rare:68 | ||||
| chr15:75625564-75625844 | Common:2; Rare:70 |