| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:29140374-29140475 | Common:3; Rare:34 | ||||
| chr17:29293788-29294017 | Common:2; Rare:85 | ||||
| chr17:29294094-29294338 | Common:3; Rare:99 | ||||
| chr17:29390225-29390427 | Common:1; Rare:61 | ||||
| chr17:29390781-29390980 | Rare:59 | ||||
| chr17:29566993-29567305 | Rare:76 | ||||
| chr17:29567794-29568093 | Common:1; Rare:62 | ||||
| chr17:29568497-29568740 | Common:4; Rare:80 | ||||
| chr17:29760839-29761063 | Rare:52 | ||||
| chr17:29761068-29761239 | Common:2; Rare:79 | ||||
| chr17:29761258-29761466 | Common:4; Rare:87 | ||||
| chr17:29929561-29929909 | Common:1; Rare:84 | ||||
| chr17:29930026-29930259 | Rare:63 | ||||
| chr17:30235615-30235984 | Common:2; Rare:83; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:30291918-30292163 | Common:1; Rare:88 |