| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:71604840-71604927 | Rare:11 | ||||
| chr15:71744176-71744448 | Common:3; Rare:48 | ||||
| chr15:71768295-71768551 | Rare:39 | ||||
| chr15:71818258-71818388 | Rare:17 | ||||
| chr15:71841643-71841790 | Common:1; Rare:16 | ||||
| chr15:71905411-71905559 | Rare:29 | ||||
| chr15:71933638-71933693 | Rare:14 | ||||
| chr15:72205312-72205637 | Common:2; Rare:58 | ||||
| chr15:72237525-72237721 | Rare:34 | ||||
| chr15:72325235-72325523 | Rare:31 | ||||
| chr15:72344082-72344367 | Rare:61; Clinvar (benign):1 | ||||
| chr15:72364754-72364806 | Rare:10 | ||||
| chr15:72374584-72374976 | Common:1; Rare:59 | ||||
| chr15:72507818-72508088 | Common:1; Rare:47 | ||||
| chr15:72529485-72529561 | Rare:14 |