| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35142257-35142329 | Common:1; Rare:30 | ||||
| chr17:35242898-35243123 | Rare:78 | ||||
| chr17:35373474-35373981 | Common:6; Rare:104 | ||||
| chr17:35373990-35374061 | Common:1; Rare:18 | ||||
| chr17:35432361-35432754 | Common:3; Rare:68 | ||||
| chr17:35448195-35448395 | Common:1; Rare:46 | ||||
| chr17:35487193-35487403 | Rare:44 | ||||
| chr17:35487529-35487638 | Rare:19 | ||||
| chr17:35487800-35487899 | Rare:32 | ||||
| chr17:35578488-35578796 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35578861-35578951 | Rare:14 | ||||
| chr17:35586928-35587548 | Common:3; Rare:142 | ||||
| chr17:35587565-35587603 | Rare:10 | ||||
| chr17:35587773-35587858 | Rare:9 | ||||
| chr17:35731539-35731682 | Rare:41 |