| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7484697-7484854 | Rare:61 | ||||
| chr17:7549006-7549237 | Common:3; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558137-7558325 | Common:1; Rare:36 | ||||
| chr17:7558388-7558783 | Rare:81 | ||||
| chr17:7558950-7559040 | Rare:19 | ||||
| chr17:7561766-7562008 | Common:2; Rare:68 | ||||
| chr17:7576231-7576841 | Common:3; Rare:184 | ||||
| chr17:7579363-7579722 | Common:1; Rare:121 | ||||
| chr17:7583487-7583876 | Common:1; Rare:155; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584068-7584099 | Rare:7 | ||||
| chr17:7626760-7627061 | Common:2; Rare:78 | ||||
| chr17:7627455-7627561 | Common:1; Rare:31 | ||||
| chr17:7627635-7627969 | Common:3; Rare:119 | ||||
| chr17:7686402-7686677 | Rare:69 | ||||
| chr17:7687456-7687569 | Rare:30; Clinvar:1 |