| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4806996-4807210 | Common:4; Rare:67 | ||||
| chr17:4833159-4833543 | Rare:101 | ||||
| chr17:4899379-4899460 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:4939916-4940373 | Common:2; Rare:135 | ||||
| chr17:4948945-4949165 | Common:1; Rare:79 | ||||
| chr17:4949828-4950175 | Common:1; Rare:83 | ||||
| chr17:4967748-4967923 | Rare:70 | ||||
| chr17:4969292-4969440 | Rare:47 | ||||
| chr17:4969631-4969841 | Rare:62 | ||||
| chr17:4987635-4987819 | Common:2; Rare:63 | ||||
| chr17:4997952-4998154 | Common:2; Rare:81; Clinvar (benign):1 | ||||
| chr17:5078342-5078518 | Common:4; Rare:50 | ||||
| chr17:5191831-5192077 | Common:1; Rare:80 | ||||
| chr17:5234804-5234983 | Rare:39 | ||||
| chr17:5282084-5282292 | Common:9; Rare:103 |