| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61954931-61955613 | Common:10; Rare:168; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:61966498-61966948 | Common:2; Rare:195 | ||||
| chr11:61966877-61967371 | Common:3; Rare:204 | ||||
| chr11:61967340-61968052 | Common:35; Rare:1049; Clinvar:24 | ||||
| chr11:62123665-62124166 | Common:48; Rare:666 | ||||
| chr11:62124470-62124850 | Common:6; Rare:104 | ||||
| chr11:62337197-62337617 | Common:17; Rare:290 | ||||
| chr11:62418157-62418557 | Common:3; Rare:69 | ||||
| chr11:62535751-62536414 | Common:9; Rare:266 | ||||
| chr11:62545291-62546178 | Common:8; Rare:727 | ||||
| chr11:62546139-62547079 | Common:3; Rare:665 | ||||
| chr11:62555812-62556212 | Common:1; Rare:99 | ||||
| chr11:62572720-62573336 | Common:3; Rare:211 | ||||
| chr11:62573752-62574313 | Rare:614 | ||||
| chr11:62591420-62592010 | Rare:875 |