| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1455955-1456011 | Rare:9 | ||||
| chr17:1456245-1456587 | Common:7; Rare:128 | ||||
| chr17:1474614-1474852 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr17:1484823-1485229 | Common:1; Rare:102 | ||||
| chr17:1485271-1485404 | Common:2; Rare:34 | ||||
| chr17:1485989-1486104 | Common:1; Rare:24 | ||||
| chr17:1486384-1486524 | Common:1; Rare:49 | ||||
| chr17:1486902-1487138 | Rare:55 | ||||
| chr17:1487200-1487349 | Common:1; Rare:45 | ||||
| chr17:1491173-1491408 | Common:1; Rare:65 | ||||
| chr17:1491675-1491794 | Common:1; Rare:37 | ||||
| chr17:1516557-1517018 | Common:3; Rare:158 | ||||
| chr17:1562290-1562556 | Common:1; Rare:60 | ||||
| chr17:1562701-1563008 | Common:3; Rare:103 | ||||
| chr17:1628339-1628583 | Rare:79 |