| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41115958-41116061 | Rare:31 | ||||
| chr15:41116075-41116437 | Common:4; Rare:176 | ||||
| chr15:41116442-41116708 | Common:1; Rare:123 | ||||
| chr15:41230709-41230850 | Rare:43 | ||||
| chr15:41231206-41231362 | Rare:52 | ||||
| chr15:41402382-41402593 | Common:7; Rare:119; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:41416883-41417196 | Common:8; Rare:231 | ||||
| chr15:41493060-41493480 | Rare:194 | ||||
| chr15:41493744-41493845 | Rare:29 | ||||
| chr15:41544233-41544364 | Rare:100 | ||||
| chr15:41559101-41559245 | Common:1; Rare:37 | ||||
| chr15:41621145-41621256 | Common:1; Rare:26 | ||||
| chr15:41621161-41621880 | Common:2; Rare:258 | ||||
| chr15:41660165-41660535 | Rare:151 | ||||
| chr15:41660682-41660831 | Rare:76 |