| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42273097-42273230 | Common:1; Rare:55 | ||||
| chr15:42273394-42273487 | Rare:37 | ||||
| chr15:42548725-42548870 | Common:2; Rare:80 | ||||
| chr15:43106034-43106231 | Rare:60 | ||||
| chr15:43330516-43330726 | Common:1; Rare:75 | ||||
| chr15:43371030-43371181 | Common:1; Rare:34 | ||||
| chr15:43510731-43510954 | Rare:67 | ||||
| chr15:43746282-43746439 | Common:1; Rare:60 | ||||
| chr15:43777114-43777380 | Rare:63 | ||||
| chr15:44536863-44537192 | Common:1; Rare:116 | ||||
| chr15:44711321-44711610 | Rare:87; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711826-44711971 | Rare:29 | ||||
| chr15:44728869-44729128 | Common:1; Rare:52 | ||||
| chr15:45023052-45023248 | Common:3; Rare:53 | ||||
| chr15:45114135-45114329 | Common:2; Rare:41 |