| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102347076-102347463 | Common:7; Rare:106 | ||||
| chr11:102452511-102452943 | Common:2; Rare:142 | ||||
| chr11:103092028-103092278 | Common:2; Rare:80 | ||||
| chr11:103109285-103109571 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:104163942-104164269 | Common:2; Rare:93 | ||||
| chr11:104164274-104164392 | Common:2; Rare:32 | ||||
| chr11:105609977-105610406 | Common:1; Rare:86 | ||||
| chr11:105610576-105610767 | Rare:41 | ||||
| chr11:106077289-106077730 | Common:2; Rare:138 | ||||
| chr11:107457734-107457932 | Common:2; Rare:70 | ||||
| chr11:107565706-107565781 | Rare:22 | ||||
| chr11:108008779-108009040 | Common:1; Rare:73 | ||||
| chr11:108009247-108009276 | Rare:15 | ||||
| chr11:108009284-108009394 | Rare:50 | ||||
| chr11:108121388-108121665 | Common:5; Rare:99; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 |