| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41231110-41231379 | Rare:94 | ||||
| chr15:41402385-41402538 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:41416960-41417213 | Common:4; Rare:112 | ||||
| chr15:41544243-41544355 | Rare:47 | ||||
| chr15:41621419-41621548 | Common:1; Rare:27 | ||||
| chr15:41660302-41660535 | Rare:74 | ||||
| chr15:41774304-41774751 | Common:1; Rare:119 | ||||
| chr15:41827932-41828127 | Common:3; Rare:64 | ||||
| chr15:41972494-41972875 | Common:2; Rare:107 | ||||
| chr15:42208225-42208401 | Rare:57 | ||||
| chr15:42272997-42273276 | Common:1; Rare:105 | ||||
| chr15:42273394-42273687 | Rare:98 | ||||
| chr15:42457501-42457732 | Rare:46 | ||||
| chr15:42490993-42491261 | Common:1; Rare:74 | ||||
| chr15:42495493-42495694 | Common:2; Rare:58 |