| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143937189-143937320 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:143937809-143937866 | Rare:8 | ||||
| chr8:143938142-143938345 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):4 | ||||
| chr8:143952211-143952298 | Common:5; Rare:38 | ||||
| chr8:143978031-143978218 | Rare:42 | ||||
| chr8:144093604-144093803 | Rare:22 | ||||
| chr8:144397604-144397874 | Common:1; Rare:114 | ||||
| chr8:144506587-144506754 | Common:4; Rare:107 | ||||
| chr8:144508250-144508289 | Rare:8 | ||||
| chr8:144700482-144700686 | Common:3; Rare:45 | ||||
| chr8:145002835-145003056 | Common:2; Rare:76 | ||||
| chr9:503928-504093 | Common:3; Rare:46 | ||||
| chr9:693477-693750 | Rare:63 | ||||
| chr9:738043-738411 | Common:3; Rare:149; Clinvar:1 | ||||
| chr9:742108-742268 | Common:1; Rare:73 |