| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15262460-15262827 | Rare:75 | ||||
| chr17:15699521-15699789 | Common:3; Rare:73 | ||||
| chr17:15999598-16000028 | Common:3; Rare:184; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16040463-16040667 | Common:2; Rare:32 | ||||
| chr17:16217086-16217240 | Rare:42; Clinvar:1 | ||||
| chr17:16380577-16380814 | Common:4; Rare:58 | ||||
| chr17:17496388-17496580 | Common:2; Rare:51 | ||||
| chr17:17591582-17591911 | Common:2; Rare:92 | ||||
| chr17:17972522-17972892 | Common:1; Rare:95 | ||||
| chr17:18183046-18183111 | Rare:24 | ||||
| chr17:18183761-18183931 | Rare:74 | ||||
| chr17:18254577-18254824 | Rare:86 | ||||
| chr17:18314925-18315308 | Common:1; Rare:107 | ||||
| chr17:18682211-18682465 | Common:8; Rare:26 | ||||
| chr17:18781097-18781318 | Common:4; Rare:61 |