| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7857147-7857735 | Common:4; Rare:237 | ||||
| chr17:7857918-7858072 | Rare:55 | ||||
| chr17:7885187-7885337 | Rare:41 | ||||
| chr17:7931890-7932258 | Common:5; Rare:99 | ||||
| chr17:8152355-8152567 | Common:2; Rare:51 | ||||
| chr17:8162911-8163079 | Rare:52 | ||||
| chr17:8248042-8248136 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8435647-8436006 | Common:5; Rare:148 | ||||
| chr17:9576605-9576692 | Rare:19 | ||||
| chr17:10697503-10697653 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:14069395-14069556 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:15699497-15699773 | Common:3; Rare:72 | ||||
| chr17:15999593-16000028 | Common:3; Rare:185; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16217073-16217235 | Rare:41; Clinvar:1 | ||||
| chr17:17591589-17591926 | Common:2; Rare:96 |