| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151083445-151083606 | Common:1; Rare:36 | ||||
| chr7:151232211-151232510 | Common:2; Rare:74 | ||||
| chr7:151877142-151877506 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:155644384-155644810 | Common:4; Rare:138 | ||||
| chr7:157336760-157337141 | Common:3; Rare:181; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158704800-158705135 | Common:1; Rare:109 | ||||
| chr8:232176-232462 | Common:3; Rare:119 | ||||
| chr8:406828-406991 | Rare:67 | ||||
| chr8:2127721-2127809 | Common:3; Rare:32 | ||||
| chr8:6406552-6406685 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563225-6563279 | Common:1; Rare:10 | ||||
| chr8:11802450-11802825 | Common:6; Rare:203 | ||||
| chr8:12754046-12754189 | Common:1; Rare:57 | ||||
| chr8:17246787-17247048 | Common:2; Rare:113 | ||||
| chr8:17801092-17801344 | Common:7; Rare:96 |