| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:38967330-38967670 | Common:3; Rare:190 | ||||
| chr17:39197540-39197803 | Common:1; Rare:99 | ||||
| chr17:39199962-39200374 | Common:6; Rare:267 | ||||
| chr17:39401560-39401859 | Common:2; Rare:127 | ||||
| chr17:39401794-39402556 | Common:13; Rare:265 | ||||
| chr17:39402475-39402591 | Common:1; Rare:46 | ||||
| chr17:39451176-39451417 | Common:6; Rare:143 | ||||
| chr17:39461232-39461711 | Common:3; Rare:185 | ||||
| chr17:39461790-39462070 | Common:6; Rare:112 | ||||
| chr17:39637004-39637210 | Common:7; Rare:123 | ||||
| chr17:39637230-39637500 | Common:3; Rare:127 | ||||
| chr17:39687670-39687920 | Rare:158; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:39687940-39688280 | Rare:158 | ||||
| chr17:39699900-39700071 | Rare:71 | ||||
| chr17:39730233-39730577 | Common:1; Rare:113 |