| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42581913-42582137 | Common:3; Rare:69 | ||||
| chr3:42582255-42582339 | Rare:23 | ||||
| chr3:42600398-42600761 | Common:2; Rare:138 | ||||
| chr3:42630834-42631294 | Common:1; Rare:85 | ||||
| chr3:42653672-42653704 | Rare:8 | ||||
| chr3:42654129-42654159 | Rare:6 | ||||
| chr3:42773211-42773254 | Rare:20 | ||||
| chr3:42804272-42804663 | Common:2; Rare:107 | ||||
| chr3:43621907-43622316 | Common:2; Rare:120; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690754-43690986 | Common:2; Rare:122; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338713-44338800 | Common:3; Rare:30 | ||||
| chr3:44477646-44477824 | Common:1; Rare:32 | ||||
| chr3:44624904-44625095 | Common:2; Rare:56 | ||||
| chr3:44729548-44729667 | Common:1; Rare:47 | ||||
| chr3:44761564-44761774 | Common:3; Rare:88 |