| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:11997302-11997765 | Common:4; Rare:153 | ||||
| chr17:12020690-12020966 | Common:2; Rare:118 | ||||
| chr17:13017618-13017797 | Common:1; Rare:80; Clinvar (benign):3 | ||||
| chr17:13017911-13018375 | Common:8; Rare:152; Clinvar (benign):2 | ||||
| chr17:14069271-14069745 | Common:3; Rare:158; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:14300804-14301103 | Common:2; Rare:81 | ||||
| chr17:15563538-15563787 | Common:1; Rare:75 | ||||
| chr17:15682627-15682905 | Common:1; Rare:62 | ||||
| chr17:15683295-15683371 | Rare:14 | ||||
| chr17:15684220-15684465 | Common:3; Rare:69 | ||||
| chr17:15699442-15699826 | Common:5; Rare:109 | ||||
| chr17:15999430-15999530 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:15999628-15999916 | Common:3; Rare:147; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr17:16000268-16000319 | Common:1; Rare:16 | ||||
| chr17:16214978-16215123 | Rare:46 |