| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49677410-49677810 | Rare:229 | ||||
| chr17:49677941-49678366 | Rare:257 | ||||
| chr17:49707587-49707807 | Rare:137 | ||||
| chr17:49707841-49708603 | Common:4; Rare:600 | ||||
| chr17:49764072-49764214 | Rare:51 | ||||
| chr17:49788364-49788774 | Common:4; Rare:324 | ||||
| chr17:49788917-49789393 | Common:3; Rare:162 | ||||
| chr17:49968260-49968795 | Common:6; Rare:204 | ||||
| chr17:49968950-49969320 | Common:4; Rare:171 | ||||
| chr17:49994958-49995520 | Common:13; Rare:195; Clinvar:9; Clinvar (benign):5 | ||||
| chr17:50055657-50056243 | Common:15; Rare:297 | ||||
| chr17:50056214-50056614 | Common:2; Rare:165 | ||||
| chr17:50094270-50094510 | Common:2; Rare:57 | ||||
| chr17:50095064-50095451 | Common:4; Rare:211 | ||||
| chr17:50149720-50150300 | Common:23; Rare:227; Clinvar:12 |