| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:236791-237042 | Common:3; Rare:88 | ||||
| chr11:504432-504785 | Common:3; Rare:93 | ||||
| chr11:506766-507001 | Common:2; Rare:76 | ||||
| chr11:576411-576519 | Rare:44 | ||||
| chr11:695562-695818 | Common:1; Rare:65 | ||||
| chr11:777460-777619 | Common:1; Rare:70 | ||||
| chr11:832703-833014 | Common:7; Rare:95 | ||||
| chr11:842454-842974 | Common:8; Rare:217 | ||||
| chr11:843964-844159 | Common:1; Rare:47 | ||||
| chr11:1763866-1764108 | Common:3; Rare:106; Clinvar:3; Clinvar (benign):6 | ||||
| chr11:1853074-1853139 | Rare:20 | ||||
| chr11:1919450-1919729 | Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:2902065-2902296 | Common:1; Rare:49 | ||||
| chr11:3797496-3797820 | Rare:112 | ||||
| chr11:3840905-3841097 | Rare:81 |