| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1763860-1764094 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):6 | ||||
| chr11:2929259-2929474 | Common:1; Rare:78 | ||||
| chr11:3379042-3379302 | Common:3; Rare:69 | ||||
| chr11:3797433-3797971 | Rare:201 | ||||
| chr11:3840910-3841096 | Rare:78 | ||||
| chr11:3855551-3855718 | Common:2; Rare:32 | ||||
| chr11:4094592-4094921 | Common:2; Rare:92 | ||||
| chr11:5624918-5625023 | Rare:13 | ||||
| chr11:6390219-6390567 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr11:6419042-6419218 | Common:3; Rare:39 | ||||
| chr11:6481223-6481532 | Common:4; Rare:118 | ||||
| chr11:6603550-6603877 | Common:4; Rare:93; Clinvar (benign):3 | ||||
| chr11:6615170-6615579 | Common:2; Rare:112; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr11:6683122-6683642 | Common:6; Rare:198 | ||||
| chr11:7994471-7994597 | Rare:47 |