| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76376378-76376757 | Common:8; Rare:131 | ||||
| chr17:76382258-76382604 | Common:2; Rare:129 | ||||
| chr17:76382838-76383287 | Rare:175 | ||||
| chr17:76383658-76383872 | Common:2; Rare:82 | ||||
| chr17:76384304-76384797 | Common:9; Rare:246 | ||||
| chr17:76453134-76453319 | Rare:58 | ||||
| chr17:76501321-76501547 | Rare:139; Clinvar (benign):6 | ||||
| chr17:76551092-76551318 | Common:1; Rare:87 | ||||
| chr17:76688650-76689000 | Common:5; Rare:83 | ||||
| chr17:76725735-76726107 | Common:2; Rare:196 | ||||
| chr17:76726402-76726962 | Common:10; Rare:393 | ||||
| chr17:76737270-76737744 | Common:9; Rare:332 | ||||
| chr17:76737830-76738123 | Common:8; Rare:165 | ||||
| chr17:77088578-77088870 | Common:3; Rare:146 | ||||
| chr17:77140575-77141067 | Common:8; Rare:322 |