| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5419608-5420266 | Common:6; Rare:221 | ||||
| chr17:5438915-5439047 | Rare:41 | ||||
| chr17:5486136-5486654 | Common:5; Rare:176 | ||||
| chr17:5486801-5486919 | Common:4; Rare:35 | ||||
| chr17:6444169-6444466 | Common:2; Rare:92 | ||||
| chr17:6640646-6641085 | Common:7; Rare:134 | ||||
| chr17:6651574-6651672 | Common:1; Rare:28 | ||||
| chr17:7012315-7012686 | Rare:128 | ||||
| chr17:7204392-7204488 | Rare:29 | ||||
| chr17:7204882-7204912 | Rare:4 | ||||
| chr17:7219710-7219949 | Common:3; Rare:91; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:7234472-7234637 | Common:2; Rare:90 | ||||
| chr17:7242272-7242590 | Common:1; Rare:105 | ||||
| chr17:7251972-7252321 | Common:1; Rare:133 | ||||
| chr17:7306873-7307068 | Common:1; Rare:61 |