| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70096205-70096381 | Rare:51 | ||||
| chr15:70763398-70763732 | Common:2; Rare:107 | ||||
| chr15:71547271-71547365 | Rare:25 | ||||
| chr15:72117748-72118425 | Common:5; Rare:225 | ||||
| chr15:72231123-72231440 | Common:3; Rare:104 | ||||
| chr15:72375951-72376124 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:72474327-72474620 | Rare:105 | ||||
| chr15:73926330-73926471 | Rare:40 | ||||
| chr15:73994587-73994783 | Rare:41 | ||||
| chr15:74173604-74173906 | Common:3; Rare:72 | ||||
| chr15:74461107-74461323 | Rare:65 | ||||
| chr15:74540966-74541268 | Common:3; Rare:107 | ||||
| chr15:74598266-74598511 | Common:1; Rare:102 | ||||
| chr15:74615622-74615898 | Common:3; Rare:92 | ||||
| chr15:74618990-74619303 | Common:2; Rare:84 |