| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6652095-6652268 | Common:5; Rare:62 | ||||
| chr17:6652284-6652433 | Rare:44 | ||||
| chr17:7012267-7012687 | Rare:139 | ||||
| chr17:7013328-7013453 | Rare:44 | ||||
| chr17:7014561-7015154 | Common:6; Rare:209 | ||||
| chr17:7035727-7036217 | Common:3; Rare:111 | ||||
| chr17:7177478-7177716 | Common:1; Rare:61 | ||||
| chr17:7219754-7219995 | Common:3; Rare:97; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:7220257-7220755 | Common:2; Rare:160; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr17:7234355-7234639 | Common:2; Rare:132 | ||||
| chr17:7237767-7237988 | Common:1; Rare:67 | ||||
| chr17:7238005-7238031 | Rare:5 | ||||
| chr17:7238556-7238714 | Common:2; Rare:11 | ||||
| chr17:7239384-7239648 | Common:2; Rare:81 | ||||
| chr17:7241786-7241916 | Common:2; Rare:28 |