| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88528673-88529156 | Common:8; Rare:110 | ||||
| chr16:88532658-88532934 | Rare:108 | ||||
| chr16:88721371-88721607 | Common:1; Rare:118; Clinvar:1 | ||||
| chr16:89833742-89834033 | Common:2; Rare:83 | ||||
| chr17:592764-592961 | Common:3; Rare:36 | ||||
| chr17:639248-639476 | Common:1; Rare:40 | ||||
| chr17:1713903-1713994 | Rare:13 | ||||
| chr17:1715245-1715462 | Rare:38 | ||||
| chr17:1774945-1775192 | Common:2; Rare:98; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:1777068-1777265 | Rare:78; Clinvar:1 | ||||
| chr17:2963802-2963878 | Rare:25 | ||||
| chr17:3647360-3647448 | Rare:15 | ||||
| chr17:3655600-3655663 | Rare:17 | ||||
| chr17:3656815-3656987 | Rare:42 | ||||
| chr17:3657785-3658100 | Common:2; Rare:110; Clinvar:3; Clinvar (pathogenic):2 |