| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34154850-34155150 | Common:4; Rare:50 | ||||
| chr15:34209330-34209910 | Common:13; Rare:252 | ||||
| chr15:34209946-34210290 | Common:12; Rare:355 | ||||
| chr15:34224268-34224668 | Common:1; Rare:77 | ||||
| chr15:34224777-34225117 | Common:2; Rare:461 | ||||
| chr15:34225067-34225467 | Common:1; Rare:110 | ||||
| chr15:34318206-34318606 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:34318740-34318970 | Common:6; Rare:144 | ||||
| chr15:34337023-34337423 | Common:3; Rare:165 | ||||
| chr15:34337670-34338320 | Common:4; Rare:574 | ||||
| chr15:34342376-34342840 | Common:6; Rare:150 | ||||
| chr15:34342907-34343413 | Common:16; Rare:312; Clinvar:12; Clinvar (benign):6 | ||||
| chr15:34366268-34366668 | Common:2; Rare:92 | ||||
| chr15:34366960-34367610 | Common:17; Rare:1012 | ||||
| chr15:34367630-34367940 | Rare:111 |