| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14810536-14810787 | Common:2; Rare:86 | ||||
| chr3:15241244-15241540 | Rare:69 | ||||
| chr3:15242887-15242993 | Rare:19 | ||||
| chr3:15271818-15272210 | Common:3; Rare:84 | ||||
| chr3:15670420-15670703 | Rare:71 | ||||
| chr3:15674303-15674548 | Common:2; Rare:46 | ||||
| chr3:16301210-16301287 | Rare:13 | ||||
| chr3:16301417-16301737 | Common:4; Rare:82 | ||||
| chr3:23285359-23285596 | Rare:38 | ||||
| chr3:23389874-23389962 | Rare:19 | ||||
| chr3:25599439-25599597 | Common:1; Rare:44 | ||||
| chr3:29283003-29283320 | Common:1; Rare:61 | ||||
| chr3:30608448-30608482 | Rare:3 | ||||
| chr3:30632213-30632535 | Common:2; Rare:76 | ||||
| chr3:30644535-30644851 | Rare:74; Clinvar:2; Clinvar (benign):5 |