| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85628339-85628643 | Common:6; Rare:102 | ||||
| chr11:85647851-85647988 | Rare:36; Clinvar:2 | ||||
| chr11:88337662-88337888 | Common:4; Rare:108; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:90223035-90223115 | Common:1; Rare:30 | ||||
| chr11:93741480-93741690 | Common:5; Rare:79 | ||||
| chr11:94493795-94494010 | Common:3; Rare:63; Clinvar (benign):1 | ||||
| chr11:94973537-94973711 | Rare:52 | ||||
| chr11:95790340-95790591 | Common:1; Rare:100 | ||||
| chr11:95923829-95924127 | Common:2; Rare:130; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389866-96390024 | Common:1; Rare:58 | ||||
| chr11:102347039-102347244 | Common:6; Rare:45 | ||||
| chr11:102452680-102452872 | Rare:60 | ||||
| chr11:106077339-106077702 | Common:2; Rare:110 | ||||
| chr11:108008843-108008955 | Rare:32 | ||||
| chr11:108009273-108009345 | Rare:36 |