| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:157336778-157337138 | Common:3; Rare:168; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158704783-158704993 | Common:1; Rare:75 | ||||
| chr7:158856423-158856687 | Common:7; Rare:94 | ||||
| chr8:232143-232482 | Common:3; Rare:144 | ||||
| chr8:233032-233214 | Common:1; Rare:40 | ||||
| chr8:2127569-2127822 | Common:9; Rare:54 | ||||
| chr8:6406518-6406689 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563180-6563334 | Common:2; Rare:38 | ||||
| chr8:6708194-6708347 | Common:2; Rare:55 | ||||
| chr8:10839810-10840149 | Common:3; Rare:114 | ||||
| chr8:11284719-11284861 | Common:2; Rare:59 | ||||
| chr8:11802450-11802996 | Common:7; Rare:302 | ||||
| chr8:12754060-12754207 | Common:1; Rare:60 | ||||
| chr8:13566760-13566911 | Common:6; Rare:58 | ||||
| chr8:15540134-15540363 | Common:5; Rare:82; Clinvar:9; Clinvar (benign):1 |