| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74170811-74171027 | Common:1; Rare:57 | ||||
| chr11:74171089-74171498 | Common:2; Rare:138 | ||||
| chr11:74398356-74398610 | Common:3; Rare:69 | ||||
| chr11:74398692-74399134 | Common:1; Rare:128 | ||||
| chr11:74466995-74467066 | Rare:11 | ||||
| chr11:74467143-74467304 | Common:6; Rare:37 | ||||
| chr11:74467474-74467624 | Common:3; Rare:35 | ||||
| chr11:74467665-74467814 | Common:1; Rare:30 | ||||
| chr11:74492986-74493063 | Common:1; Rare:11 | ||||
| chr11:74493065-74493432 | Common:1; Rare:138; Clinvar (pathogenic):1 | ||||
| chr11:74493566-74493925 | Common:1; Rare:133; Clinvar (pathogenic):1 | ||||
| chr11:74592451-74592740 | Common:1; Rare:85 | ||||
| chr11:74592823-74592929 | Rare:16 | ||||
| chr11:74592993-74593178 | Rare:36 | ||||
| chr11:74748630-74748968 | Common:3; Rare:107 |