| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78840694-78841127 | Common:4; Rare:302 | ||||
| chr17:78979841-78980103 | Common:4; Rare:104 | ||||
| chr17:79009695-79009938 | Common:18; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:79074619-79075009 | Common:9; Rare:191 | ||||
| chr17:79730653-79730963 | Common:3; Rare:47 | ||||
| chr17:79731051-79731173 | Common:2; Rare:67 | ||||
| chr17:79777814-79778266 | Common:2; Rare:362 | ||||
| chr17:79797004-79797423 | Common:2; Rare:294 | ||||
| chr17:79798372-79798485 | Common:1; Rare:19 | ||||
| chr17:79839406-79839709 | Rare:155 | ||||
| chr17:79993416-79993990 | Common:2; Rare:193 | ||||
| chr17:80035826-80036069 | Common:2; Rare:148 | ||||
| chr17:80036370-80036700 | Common:5; Rare:114; Clinvar (benign):4 | ||||
| chr17:80101404-80101680 | Common:10; Rare:236; Clinvar (benign):10 | ||||
| chr17:80147139-80147383 | Common:6; Rare:89 |