| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:155644377-155644841 | Common:4; Rare:149 | ||||
| chr7:157336778-157337073 | Common:2; Rare:142; Clinvar:1 | ||||
| chr7:158856455-158856695 | Common:7; Rare:87 | ||||
| chr7:159144846-159145064 | Common:9; Rare:45 | ||||
| chr8:232174-232462 | Common:3; Rare:121 | ||||
| chr8:715887-716124 | Common:1; Rare:96 | ||||
| chr8:6406534-6406679 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563130-6563333 | Common:2; Rare:47 | ||||
| chr8:6563420-6563447 | Rare:6 | ||||
| chr8:11284737-11284861 | Common:2; Rare:55 | ||||
| chr8:11769569-11769791 | Common:5; Rare:96 | ||||
| chr8:11802507-11802771 | Common:6; Rare:136 | ||||
| chr8:11845175-11845453 | Common:4; Rare:140 | ||||
| chr8:13514648-13514785 | Common:1; Rare:35 | ||||
| chr8:13514816-13514860 | Rare:5 |