| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102415784-102415992 | Common:4; Rare:37 | ||||
| chr11:108147561-108147663 | Common:3; Rare:22; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:111539377-111539503 | Rare:23 | ||||
| chr11:111539510-111539739 | Rare:40 | ||||
| chr11:111543624-111543958 | Common:1; Rare:62 | ||||
| chr11:111563407-111563715 | Common:5; Rare:54 | ||||
| chr11:111688893-111689196 | Rare:42 | ||||
| chr11:114441231-114441538 | Common:2; Rare:51 | ||||
| chr11:117166100-117166142 | Rare:13 | ||||
| chr11:117212147-117212364 | Common:3; Rare:45 | ||||
| chr11:118392466-118392787 | Common:1; Rare:57 | ||||
| chr11:118438400-118438698 | Rare:57 | ||||
| chr11:118608558-118608846 | Rare:63 | ||||
| chr11:118619502-118619904 | Common:2; Rare:61 | ||||
| chr11:118791665-118791894 | Common:1; Rare:64 |