| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:706517-706646 | Rare:21 | ||||
| chr11:777428-777602 | Common:1; Rare:83 | ||||
| chr11:809225-809381 | Common:2; Rare:38 | ||||
| chr11:809798-810038 | Common:2; Rare:110 | ||||
| chr11:842517-842978 | Common:8; Rare:181 | ||||
| chr11:1309555-1309754 | Common:2; Rare:88 | ||||
| chr11:3057365-3057545 | Rare:64 | ||||
| chr11:6320481-6320728 | Common:2; Rare:72 | ||||
| chr11:6419063-6419216 | Common:2; Rare:38 | ||||
| chr11:6481283-6481530 | Common:4; Rare:101 | ||||
| chr11:6603561-6603825 | Common:3; Rare:84; Clinvar (benign):3 | ||||
| chr11:6683271-6683644 | Common:6; Rare:140 | ||||
| chr11:8682650-8682811 | Common:2; Rare:71 | ||||
| chr11:8964931-8965020 | Common:1; Rare:21 | ||||
| chr11:9460619-9460985 | Common:4; Rare:92 |