| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8249067-8249319 | Common:1; Rare:57 | ||||
| chr17:8295356-8295511 | Common:1; Rare:41 | ||||
| chr17:8867642-8867774 | Common:1; Rare:21 | ||||
| chr17:8965724-8965880 | Common:2; Rare:40 | ||||
| chr17:10697505-10697663 | Common:4; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:11997436-11997588 | Rare:52 | ||||
| chr17:13017662-13017773 | Rare:47; Clinvar (benign):1 | ||||
| chr17:14069457-14069542 | Common:1; Rare:29; Clinvar (benign):2 | ||||
| chr17:15999591-15999846 | Common:2; Rare:132; Clinvar:4; Clinvar (benign):5 | ||||
| chr17:16215391-16215614 | Common:1; Rare:88 | ||||
| chr17:16381022-16381450 | Common:4; Rare:185 | ||||
| chr17:16972010-16972195 | Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:17179397-17179565 | Common:2; Rare:25 | ||||
| chr17:18039014-18039410 | Common:3; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18314925-18315396 | Common:1; Rare:142 |