| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:8963435-8963787 | Common:2; Rare:79 | ||||
| chr3:9249617-9249743 | Common:1; Rare:35 | ||||
| chr3:9363010-9363098 | Rare:31 | ||||
| chr3:9749789-9749983 | Rare:61 | ||||
| chr3:9769886-9770059 | Common:1; Rare:43 | ||||
| chr3:9792414-9792570 | Rare:40 | ||||
| chr3:9792692-9793123 | Common:3; Rare:152 | ||||
| chr3:9843968-9844076 | Common:1; Rare:49 | ||||
| chr3:9933524-9933857 | Common:2; Rare:135; Clinvar:3 | ||||
| chr3:9986788-9987153 | Common:3; Rare:105 | ||||
| chr3:10026334-10026482 | Rare:42 | ||||
| chr3:11719419-11719581 | Rare:52 | ||||
| chr3:12158907-12159008 | Rare:32 | ||||
| chr3:12287647-12287961 | Common:8; Rare:67 | ||||
| chr3:12484336-12484517 | Common:4; Rare:55; Clinvar:1; Clinvar (benign):1 |