| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50292322-50292626 | Common:1; Rare:128 | ||||
| chr3:50299268-50299692 | Common:1; Rare:100 | ||||
| chr3:50303555-50303608 | Common:1; Rare:7 | ||||
| chr3:50322672-50322805 | Rare:19 | ||||
| chr3:50328172-50328349 | Rare:53 | ||||
| chr3:50350705-50350924 | Common:1; Rare:37 | ||||
| chr3:50351019-50351215 | Common:3; Rare:38 | ||||
| chr3:50359344-50359597 | Common:3; Rare:68 | ||||
| chr3:50365075-50365373 | Common:1; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:50567608-50567895 | Common:1; Rare:87 | ||||
| chr3:50569455-50569570 | Common:1; Rare:28 | ||||
| chr3:50611733-50611892 | Rare:38 | ||||
| chr3:50611971-50612331 | Common:1; Rare:83; Clinvar:1 | ||||
| chr3:51385006-51385384 | Common:2; Rare:119 | ||||
| chr3:51499948-51500357 | Common:1; Rare:87 |