| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14651502-14651824 | Rare:99 | ||||
| chr3:14947233-14947582 | Common:4; Rare:158 | ||||
| chr3:15065250-15065362 | Common:2; Rare:40 | ||||
| chr3:15427486-15427652 | Common:1; Rare:59 | ||||
| chr3:15601495-15601764 | Common:4; Rare:109; Clinvar:1 | ||||
| chr3:16264851-16265243 | Common:2; Rare:136 | ||||
| chr3:16513647-16513787 | Common:4; Rare:33 | ||||
| chr3:19946894-19947219 | Common:7; Rare:115 | ||||
| chr3:23916925-23917224 | Rare:110 | ||||
| chr3:29280952-29281080 | Common:2; Rare:19 | ||||
| chr3:33097104-33097286 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33798500-33798666 | Common:2; Rare:59 | ||||
| chr3:37176104-37176374 | Common:1; Rare:71 | ||||
| chr3:38137087-38137409 | Rare:67 | ||||
| chr3:39107525-39107730 | Common:4; Rare:65 |