| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41962007-41962379 | Common:7; Rare:91 | ||||
| chr3:42013505-42013802 | Common:6; Rare:84 | ||||
| chr3:42581871-42582138 | Common:3; Rare:86 | ||||
| chr3:42582256-42582453 | Common:1; Rare:48 | ||||
| chr3:42600351-42600778 | Common:3; Rare:165 | ||||
| chr3:42600888-42601004 | Rare:45 | ||||
| chr3:42630919-42631312 | Common:1; Rare:71 | ||||
| chr3:42633202-42633491 | Rare:47 | ||||
| chr3:42634349-42634686 | Rare:67 | ||||
| chr3:42654081-42654178 | Common:1; Rare:16 | ||||
| chr3:42773215-42773260 | Rare:18 | ||||
| chr3:42804426-42804671 | Common:2; Rare:76 | ||||
| chr3:43286239-43286673 | Common:2; Rare:142 | ||||
| chr3:43621907-43622328 | Common:2; Rare:123; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690817-43691001 | Common:3; Rare:102; Clinvar:7; Clinvar (benign):2 |