| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:152676100-152676316 | Common:2; Rare:96; Clinvar (benign):6 | ||||
| chr7:155644377-155644719 | Common:2; Rare:117 | ||||
| chr7:156640535-156640791 | Common:3; Rare:121 | ||||
| chr7:157336749-157337069 | Common:2; Rare:153; Clinvar:1 | ||||
| chr7:158704737-158704949 | Common:1; Rare:75 | ||||
| chr7:158856423-158856680 | Common:6; Rare:93 | ||||
| chr8:232214-232403 | Common:2; Rare:72 | ||||
| chr8:2127617-2127833 | Common:8; Rare:49 | ||||
| chr8:6406527-6406668 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708179-6708341 | Common:2; Rare:62 | ||||
| chr8:6835514-6835552 | Rare:16 | ||||
| chr8:11284741-11284861 | Common:2; Rare:54 | ||||
| chr8:11474698-11474865 | Common:3; Rare:41 | ||||
| chr8:11802401-11802831 | Common:7; Rare:250 | ||||
| chr8:17246588-17247048 | Common:5; Rare:196 |