| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19648020-19648150 | Rare:29 | ||||
| chr17:19648602-19648967 | Common:3; Rare:124 | ||||
| chr17:19977804-19977999 | Common:1; Rare:65 | ||||
| chr17:20155838-20156109 | Common:1; Rare:87 | ||||
| chr17:20868211-20868591 | Common:3; Rare:107 | ||||
| chr17:21043399-21043550 | Common:2; Rare:59 | ||||
| chr17:21214144-21214359 | Common:2; Rare:97 | ||||
| chr17:21574424-21574562 | Common:1; Rare:27 | ||||
| chr17:27293927-27294167 | Common:2; Rare:100 | ||||
| chr17:27294409-27294479 | Common:1; Rare:16 | ||||
| chr17:28041064-28041358 | Common:2; Rare:52 | ||||
| chr17:28318882-28319363 | Common:3; Rare:171 | ||||
| chr17:28335381-28335836 | Common:1; Rare:110 | ||||
| chr17:28357294-28357725 | Common:11; Rare:191; Clinvar (pathogenic):1 | ||||
| chr17:28371359-28371755 | Common:5; Rare:74 |