| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7484232-7484372 | Common:1; Rare:57 | ||||
| chr17:7687468-7687580 | Rare:26 | ||||
| chr17:7857466-7857704 | Common:2; Rare:76 | ||||
| chr17:7931898-7932258 | Common:5; Rare:99 | ||||
| chr17:8176343-8176474 | Rare:39 | ||||
| chr17:10697503-10697653 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:14069368-14069580 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:15699595-15699768 | Common:2; Rare:47 | ||||
| chr17:15999671-16000025 | Common:3; Rare:143; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr17:17591626-17591967 | Common:1; Rare:99 | ||||
| chr17:18314906-18315293 | Common:1; Rare:109 | ||||
| chr17:18781091-18781299 | Common:5; Rare:58 | ||||
| chr17:18856168-18856362 | Common:1; Rare:35 | ||||
| chr17:21214144-21214341 | Common:2; Rare:87 | ||||
| chr17:27293958-27294132 | Common:1; Rare:73 |