| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5433365-5433769 | Common:1; Rare:102; Clinvar (pathogenic):3 | ||||
| chr17:5438843-5439044 | Rare:64 | ||||
| chr17:5439083-5439391 | Common:4; Rare:82 | ||||
| chr17:5486111-5486636 | Common:6; Rare:179 | ||||
| chr17:5486773-5486917 | Common:4; Rare:46 | ||||
| chr17:6444142-6444462 | Common:2; Rare:95 | ||||
| chr17:6640646-6641085 | Common:7; Rare:134 | ||||
| chr17:6651524-6651758 | Common:1; Rare:84 | ||||
| chr17:7012301-7012507 | Rare:51 | ||||
| chr17:7012519-7012758 | Rare:95 | ||||
| chr17:7013071-7013513 | Common:2; Rare:118 | ||||
| chr17:7035800-7036026 | Rare:56 | ||||
| chr17:7219801-7219952 | Common:3; Rare:70; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7223307-7223479 | Rare:57 | ||||
| chr17:7234255-7234634 | Common:2; Rare:168 |