| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:22786094-22786366 | Common:3; Rare:70 | ||||
| chr15:22786369-22786563 | Common:1; Rare:51 | ||||
| chr15:22786597-22786946 | Common:1; Rare:128; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:22786974-22787103 | Common:1; Rare:37 | ||||
| chr15:22787237-22787341 | Common:2; Rare:28 | ||||
| chr15:22838189-22838262 | Rare:13 | ||||
| chr15:22838299-22838759 | Common:5; Rare:162 | ||||
| chr15:22838765-22839103 | Common:4; Rare:88 | ||||
| chr15:22979728-22980041 | Common:2; Rare:102 | ||||
| chr15:22980149-22980596 | Common:5; Rare:164 | ||||
| chr15:22980684-22980828 | Common:3; Rare:55 | ||||
| chr15:22980878-22981104 | Common:1; Rare:49 | ||||
| chr15:23039073-23039245 | Common:1; Rare:52 | ||||
| chr15:23039282-23039343 | Rare:20 | ||||
| chr15:23039454-23039860 | Common:1; Rare:166 |