| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7674859-7675154 | Common:1; Rare:88; Clinvar:27; Clinvar (benign):24; Clinvar (pathogenic):17 | ||||
| chr17:7686402-7686677 | Rare:69 | ||||
| chr17:7687456-7687551 | Rare:22; Clinvar:1 | ||||
| chr17:7843644-7843740 | Rare:32 | ||||
| chr17:7843927-7844204 | Common:4; Rare:84 | ||||
| chr17:7857089-7857296 | Common:1; Rare:103 | ||||
| chr17:7857372-7857711 | Common:3; Rare:110 | ||||
| chr17:7857908-7858074 | Rare:58 | ||||
| chr17:7885200-7885351 | Rare:49 | ||||
| chr17:7931869-7932248 | Common:5; Rare:100 | ||||
| chr17:8146759-8146836 | Rare:25 | ||||
| chr17:8147749-8148023 | Rare:90 | ||||
| chr17:8156309-8156692 | Common:2; Rare:114 | ||||
| chr17:8162911-8163093 | Rare:62 | ||||
| chr17:8176333-8176474 | Rare:44 |