| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16217094-16217240 | Rare:42; Clinvar:1 | ||||
| chr17:16380561-16380814 | Common:4; Rare:66 | ||||
| chr17:16381253-16381443 | Rare:74 | ||||
| chr17:16415389-16415818 | Common:4; Rare:96 | ||||
| chr17:16972039-16972195 | Rare:41; Clinvar:1 | ||||
| chr17:17237133-17237298 | Common:1; Rare:56; Clinvar (benign):2 | ||||
| chr17:17237390-17237727 | Common:4; Rare:79 | ||||
| chr17:17496377-17496503 | Rare:32 | ||||
| chr17:17591589-17591948 | Common:2; Rare:103 | ||||
| chr17:18039031-18039365 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087803-18088015 | Rare:60 | ||||
| chr17:18183013-18183111 | Rare:34 | ||||
| chr17:18183282-18183511 | Rare:58 | ||||
| chr17:18183751-18183931 | Rare:82 | ||||
| chr17:18184544-18184610 | Rare:21 |