| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5116354-5116538 | Common:2; Rare:43 | ||||
| chr17:5123087-5123444 | Rare:114 | ||||
| chr17:5191788-5192123 | Common:2; Rare:102 | ||||
| chr17:5234804-5235003 | Rare:43 | ||||
| chr17:5419599-5420225 | Common:6; Rare:206 | ||||
| chr17:5438843-5439002 | Rare:52 | ||||
| chr17:5486136-5486675 | Common:5; Rare:183 | ||||
| chr17:5486810-5486933 | Common:3; Rare:39 | ||||
| chr17:5501004-5501018 | Rare:4 | ||||
| chr17:6556416-6556712 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:6640643-6641109 | Common:7; Rare:150 | ||||
| chr17:6651553-6651774 | Common:1; Rare:78 | ||||
| chr17:6755858-6756081 | Common:4; Rare:52 | ||||
| chr17:7012317-7012758 | Rare:144 | ||||
| chr17:7035796-7036099 | Rare:71 |