| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66372405-66372545 | Rare:25 | ||||
| chr11:66438960-66439250 | Common:2; Rare:116 | ||||
| chr11:66466672-66466926 | Rare:140 | ||||
| chr11:66480157-66480455 | Common:6; Rare:149 | ||||
| chr11:66510485-66510687 | Common:6; Rare:157; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr11:66545994-66546314 | Common:6; Rare:116 | ||||
| chr11:66568558-66568771 | Common:5; Rare:62 | ||||
| chr11:66593035-66593253 | Common:2; Rare:150 | ||||
| chr11:66616376-66616680 | Common:3; Rare:177 | ||||
| chr11:66616710-66617100 | Rare:169 | ||||
| chr11:66638359-66638755 | Common:8; Rare:345 | ||||
| chr11:66677765-66678130 | Common:2; Rare:253 | ||||
| chr11:66728454-66728646 | Rare:37 | ||||
| chr11:66744592-66744905 | Common:6; Rare:228 | ||||
| chr11:66842671-66843071 | Common:2; Rare:240 |