| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13017582-13017779 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr17:13017945-13018059 | Common:2; Rare:51; Clinvar (benign):2 | ||||
| chr17:14069347-14069582 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:15260787-15261015 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr17:15999505-16000165 | Common:4; Rare:276; Clinvar:7; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr17:16041009-16041073 | Common:1; Rare:10 | ||||
| chr17:16058288-16058539 | Common:1; Rare:49 | ||||
| chr17:16080400-16080645 | Common:2; Rare:54 | ||||
| chr17:16215378-16215657 | Common:2; Rare:110 | ||||
| chr17:16217102-16217268 | Rare:60; Clinvar:2 | ||||
| chr17:16217348-16217662 | Rare:91; Clinvar:1 | ||||
| chr17:16344559-16344616 | Rare:17 | ||||
| chr17:16352999-16353263 | Rare:88 | ||||
| chr17:16381013-16381470 | Common:4; Rare:195 | ||||
| chr17:17237089-17237727 | Common:8; Rare:176; Clinvar:1; Clinvar (benign):3 |