| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:71787244-71787578 | Common:17; Rare:131 | ||||
| chr11:71928398-71929075 | Common:1; Rare:188 | ||||
| chr11:72039785-72039892 | Common:1; Rare:12 | ||||
| chr11:72040795-72041017 | Rare:48 | ||||
| chr11:72041060-72041295 | Common:1; Rare:41 | ||||
| chr11:72080367-72080861 | Common:2; Rare:117; Clinvar:9 | ||||
| chr11:72112216-72112515 | Rare:78 | ||||
| chr11:72112632-72112866 | Common:3; Rare:101 | ||||
| chr11:72224077-72224382 | Common:3; Rare:65 | ||||
| chr11:72228905-72229176 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr11:72434466-72434721 | Common:4; Rare:72; Clinvar (benign):1 | ||||
| chr11:72752377-72752536 | Common:3; Rare:48 | ||||
| chr11:72814051-72814448 | Common:4; Rare:118 | ||||
| chr11:73141901-73141996 | Common:1; Rare:31 | ||||
| chr11:73218155-73218296 | Rare:24 |