| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:157336770-157337093 | Common:3; Rare:156; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704729-158704983 | Common:1; Rare:87 | ||||
| chr7:158856423-158856716 | Common:7; Rare:104 | ||||
| chr8:232174-232482 | Common:3; Rare:129 | ||||
| chr8:233030-233077 | Rare:11 | ||||
| chr8:406708-407037 | Common:4; Rare:151 | ||||
| chr8:2127522-2127811 | Common:13; Rare:71 | ||||
| chr8:6406527-6406680 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563225-6563249 | Rare:5 | ||||
| chr8:6708162-6708242 | Common:1; Rare:31 | ||||
| chr8:9150615-9150784 | Common:1; Rare:59 | ||||
| chr8:9151530-9151882 | Common:2; Rare:132 | ||||
| chr8:9555721-9555939 | Common:5; Rare:88 | ||||
| chr8:10839814-10840095 | Common:3; Rare:93 | ||||
| chr8:11284741-11284861 | Common:2; Rare:54 |