| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109559725-109561225 | Common:28; Rare:928 | ||||
| chr4:109561180-109561291 | Rare:17 | ||||
| chr4:109702765-109703298 | Common:2; Rare:236 | ||||
| chr4:109703202-109703850 | Common:8; Rare:503 | ||||
| chr4:109728790-109729782 | Common:5; Rare:235 | ||||
| chr4:109729931-109730437 | Common:20; Rare:428 | ||||
| chr4:109730370-109730607 | Common:6; Rare:100 | ||||
| chr4:109814826-109816512 | Common:25; Rare:1126 | ||||
| chr4:109912621-109913021 | Common:5; Rare:140; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:109913163-109913573 | Common:3; Rare:159; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:110197633-110198240 | Common:20; Rare:208 | ||||
| chr4:110198470-110199470 | Common:14; Rare:910 | ||||
| chr4:112145155-112145810 | Common:11; Rare:578 | ||||
| chr4:112145800-112146264 | Common:4; Rare:167 | ||||
| chr4:112231260-112231866 | Common:19; Rare:747 |