| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61333289-61333449 | Rare:49 | ||||
| chr11:61361842-61362055 | Common:2; Rare:49; Clinvar:2 | ||||
| chr11:61362243-61362410 | Common:2; Rare:50; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61429920-61430148 | Common:1; Rare:102; Clinvar (benign):3 | ||||
| chr11:61792564-61792944 | Common:5; Rare:103 | ||||
| chr11:61816760-61816981 | Rare:65 | ||||
| chr11:61967164-61967578 | Common:1; Rare:142; Clinvar:1 | ||||
| chr11:61967580-61967806 | Common:2; Rare:87; Clinvar:3 | ||||
| chr11:62123818-62124065 | Common:6; Rare:62 | ||||
| chr11:62545583-62545883 | Common:1; Rare:69 | ||||
| chr11:62546660-62546890 | Common:1; Rare:71 | ||||
| chr11:62591567-62591636 | Rare:28 | ||||
| chr11:62601640-62601738 | Rare:26 | ||||
| chr11:62611698-62611860 | Rare:37 | ||||
| chr11:62665075-62665418 | Common:5; Rare:156 |