| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7573557-7573831 | Common:2; Rare:100 | ||||
| chr17:7577401-7577715 | Rare:79 | ||||
| chr17:7583508-7583647 | Rare:49 | ||||
| chr17:7583701-7583898 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584057-7584352 | Common:1; Rare:71 | ||||
| chr17:7591965-7592214 | Common:1; Rare:37 | ||||
| chr17:7614443-7614582 | Rare:27 | ||||
| chr17:7614834-7614951 | Rare:46 | ||||
| chr17:7686402-7686680 | Rare:71 | ||||
| chr17:7687355-7687451 | Rare:20; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:7687477-7687605 | Rare:28 | ||||
| chr17:7843502-7843740 | Rare:77 | ||||
| chr17:7843971-7844248 | Common:4; Rare:78 | ||||
| chr17:7856720-7857020 | Rare:107 | ||||
| chr17:7857167-7857304 | Common:1; Rare:79 |