| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61362069-61362441 | Common:2; Rare:106; Clinvar:9; Clinvar (benign):1 | ||||
| chr11:61429863-61430161 | Common:1; Rare:124; Clinvar:3; Clinvar (benign):4 | ||||
| chr11:61792554-61792986 | Common:6; Rare:128 | ||||
| chr11:61816103-61816353 | Rare:68 | ||||
| chr11:61816982-61817285 | Common:2; Rare:53 | ||||
| chr11:61828225-61828329 | Rare:27 | ||||
| chr11:61878232-61878310 | Common:1; Rare:26 | ||||
| chr11:61891177-61891249 | Rare:14 | ||||
| chr11:61967429-61967666 | Common:2; Rare:103; Clinvar:3 | ||||
| chr11:62545583-62546011 | Common:1; Rare:99 | ||||
| chr11:62601040-62601550 | Common:3; Rare:140 | ||||
| chr11:62601610-62602216 | Common:2; Rare:171 | ||||
| chr11:62611427-62611865 | Rare:117 | ||||
| chr11:62612462-62612869 | Common:5; Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:62626334-62626587 | Common:1; Rare:74; Clinvar (pathogenic):1 |