| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7579311-7579650 | Common:1; Rare:112 | ||||
| chr17:7583508-7583881 | Common:1; Rare:147; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7627807-7627995 | Common:2; Rare:59 | ||||
| chr17:7857467-7858089 | Common:4; Rare:200 | ||||
| chr17:7931912-7932246 | Common:5; Rare:90 | ||||
| chr17:10697512-10697643 | Common:3; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:13018012-13018240 | Common:3; Rare:53 | ||||
| chr17:14069457-14069528 | Common:1; Rare:26; Clinvar (benign):2 | ||||
| chr17:15999572-15999863 | Common:3; Rare:151; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:17237095-17237415 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:18039144-18039403 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chr17:18183733-18183905 | Rare:80 | ||||
| chr17:18314907-18315332 | Common:1; Rare:120 | ||||
| chr17:18856264-18856362 | Rare:19 | ||||
| chr17:19378160-19378546 | Common:2; Rare:93 |