| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42600337-42600757 | Common:3; Rare:164 | ||||
| chr3:42773229-42773345 | Common:1; Rare:29 | ||||
| chr3:42804426-42804635 | Common:2; Rare:61 | ||||
| chr3:42936290-42936422 | Common:1; Rare:39 | ||||
| chr3:43621919-43622323 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690728-43690993 | Common:5; Rare:133; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338086-44338183 | Common:2; Rare:35 | ||||
| chr3:44338651-44338800 | Common:3; Rare:56 | ||||
| chr3:44477609-44477780 | Common:1; Rare:44 | ||||
| chr3:44510606-44510761 | Common:1; Rare:31 | ||||
| chr3:44584563-44584992 | Rare:86 | ||||
| chr3:44624929-44625095 | Common:2; Rare:45 | ||||
| chr3:44648647-44648804 | Rare:40 | ||||
| chr3:44712563-44712720 | Common:1; Rare:58 | ||||
| chr3:44729521-44729667 | Common:1; Rare:57 |