| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:518727-519087 | Common:10; Rare:194 | ||||
| chr11:536324-536648 | Common:3; Rare:79 | ||||
| chr11:554983-555360 | Common:13; Rare:173 | ||||
| chr11:568131-568248 | Common:1; Rare:36 | ||||
| chr11:568359-569026 | Common:5; Rare:247 | ||||
| chr11:571311-571413 | Common:1; Rare:22 | ||||
| chr11:588197-588329 | Common:1; Rare:25 | ||||
| chr11:696558-696694 | Common:1; Rare:31 | ||||
| chr11:707805-708247 | Common:1; Rare:113 | ||||
| chr11:712824-713127 | Common:3; Rare:56 | ||||
| chr11:738011-738304 | Rare:60 | ||||
| chr11:777998-778245 | Common:1; Rare:63 | ||||
| chr11:783654-783742 | Rare:32 | ||||
| chr11:819722-819849 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:819999-820291 | Common:2; Rare:68 |