| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18857926-18858190 | Common:5; Rare:65 | ||||
| chr17:19362565-19362660 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:19362665-19362773 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr17:19377638-19377774 | Common:2; Rare:36 | ||||
| chr17:19378162-19378537 | Common:2; Rare:92 | ||||
| chr17:19648492-19648797 | Common:3; Rare:89 | ||||
| chr17:19977778-19977877 | Rare:25 | ||||
| chr17:21214144-21214353 | Common:2; Rare:94 | ||||
| chr17:27293992-27294132 | Common:1; Rare:60 | ||||
| chr17:28318911-28319281 | Common:3; Rare:134 | ||||
| chr17:28335371-28335824 | Common:1; Rare:108 | ||||
| chr17:28357400-28357680 | Common:6; Rare:137 | ||||
| chr17:28571504-28571664 | Rare:37 | ||||
| chr17:28576879-28577054 | Common:2; Rare:49 | ||||
| chr17:28598980-28599165 | Common:2; Rare:59 |