| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41332277-41332384 | Common:1; Rare:54 | ||||
| chr15:41332437-41332951 | Common:2; Rare:211 | ||||
| chr15:41333125-41333231 | Rare:16 | ||||
| chr15:41402310-41402650 | Common:4; Rare:114; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:41402901-41403054 | Rare:27 | ||||
| chr15:41416720-41416782 | Rare:13 | ||||
| chr15:41416920-41417212 | Common:4; Rare:128 | ||||
| chr15:41493565-41493933 | Rare:98 | ||||
| chr15:41544177-41544406 | Common:2; Rare:81 | ||||
| chr15:41621160-41621267 | Common:1; Rare:30 | ||||
| chr15:41660251-41660543 | Rare:88 | ||||
| chr15:41660638-41660842 | Rare:64 | ||||
| chr15:41774031-41774957 | Common:3; Rare:241 | ||||
| chr15:41827906-41828198 | Common:4; Rare:111 | ||||
| chr15:41972519-41972912 | Common:2; Rare:101 |