| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37862216-37862616 | Common:2; Rare:114 | ||||
| chr3:37987739-37988172 | Common:8; Rare:182 | ||||
| chr3:37992804-37993204 | Rare:66 | ||||
| chr3:37993242-37993642 | Common:7; Rare:143 | ||||
| chr3:37993651-37994314 | Common:6; Rare:670 | ||||
| chr3:37994248-37994680 | Rare:615 | ||||
| chr3:37998241-37999944 | Common:41; Rare:1542 | ||||
| chr3:38008967-38009367 | Common:2; Rare:193; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:38018937-38019441 | Rare:237 | ||||
| chr3:38024403-38024803 | Common:6; Rare:518 | ||||
| chr3:38024810-38025350 | Common:16; Rare:302 | ||||
| chr3:38136623-38137065 | Common:2; Rare:222 | ||||
| chr3:38136988-38137597 | Common:5; Rare:672 | ||||
| chr3:38137886-38138286 | Rare:54 | ||||
| chr3:38138350-38138736 | Common:10; Rare:358; Clinvar:5; Clinvar (pathogenic):5 |