| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18253360-18253661 | Rare:107 | ||||
| chr17:18254524-18254838 | Rare:109 | ||||
| chr17:18260352-18260680 | Rare:89 | ||||
| chr17:18314898-18315348 | Common:1; Rare:128 | ||||
| chr17:18315668-18315795 | Rare:35 | ||||
| chr17:18363383-18363714 | Common:5; Rare:109 | ||||
| chr17:18781103-18781316 | Common:4; Rare:59 | ||||
| chr17:18856195-18856362 | Common:1; Rare:27 | ||||
| chr17:18857926-18858190 | Common:5; Rare:65 | ||||
| chr17:19362674-19363010 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr17:19377635-19377774 | Common:2; Rare:36 | ||||
| chr17:19377880-19378033 | Common:1; Rare:39 | ||||
| chr17:19378116-19378537 | Common:2; Rare:103 | ||||
| chr17:19387156-19387503 | Common:2; Rare:82 | ||||
| chr17:19533756-19533926 | Common:3; Rare:53 |