| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7251967-7252314 | Common:1; Rare:133 | ||||
| chr17:7262434-7262642 | Rare:46 | ||||
| chr17:7315101-7315417 | Common:4; Rare:111 | ||||
| chr17:7351606-7351743 | Rare:27 | ||||
| chr17:7352051-7352207 | Rare:49 | ||||
| chr17:7438183-7438298 | Rare:27 | ||||
| chr17:7479485-7479730 | Common:1; Rare:43 | ||||
| chr17:7484214-7484370 | Common:1; Rare:61 | ||||
| chr17:7558830-7559027 | Common:1; Rare:44 | ||||
| chr17:7561796-7561991 | Common:2; Rare:52 | ||||
| chr17:7576228-7576646 | Common:2; Rare:119 | ||||
| chr17:7577055-7577278 | Common:1; Rare:51 | ||||
| chr17:7583505-7583858 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7584073-7584114 | Rare:8 | ||||
| chr17:7857383-7857686 | Common:3; Rare:103 |