| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40317969-40318433 | Common:5; Rare:257 | ||||
| chr17:40322102-40322688 | Common:1; Rare:153 | ||||
| chr17:40341898-40342298 | Common:4; Rare:276 | ||||
| chr17:40363249-40363600 | Common:8; Rare:198 | ||||
| chr17:40363551-40363940 | Common:2; Rare:167 | ||||
| chr17:40417836-40418288 | Rare:368 | ||||
| chr17:40442737-40443105 | Common:4; Rare:147 | ||||
| chr17:40443200-40444068 | Common:10; Rare:596 | ||||
| chr17:40501570-40501740 | Rare:73 | ||||
| chr17:40560230-40560636 | Common:7; Rare:223 | ||||
| chr17:40647725-40648366 | Common:1; Rare:157 | ||||
| chr17:40818793-40819451 | Common:36; Rare:786; Clinvar (benign):5 | ||||
| chr17:40936544-40937235 | Common:23; Rare:316 | ||||
| chr17:40937390-40937860 | Common:12; Rare:101 | ||||
| chr17:40984151-40984280 | Common:1; Rare:44 |