| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8964372-8964522 | Common:3; Rare:48 | ||||
| chr11:8964931-8965013 | Common:1; Rare:21 | ||||
| chr11:9003972-9004151 | Common:1; Rare:68 | ||||
| chr11:9460620-9460942 | Common:3; Rare:81 | ||||
| chr11:10304801-10305085 | Common:1; Rare:62 | ||||
| chr11:10541157-10541345 | Rare:67 | ||||
| chr11:10751157-10751321 | Rare:52 | ||||
| chr11:10800194-10800629 | Rare:120 | ||||
| chr11:10800631-10800760 | Common:1; Rare:43 | ||||
| chr11:10802166-10802433 | Common:1; Rare:69 | ||||
| chr11:10858030-10858236 | Common:2; Rare:58 | ||||
| chr11:12110367-12110632 | Rare:68 | ||||
| chr11:12377468-12377638 | Rare:70 | ||||
| chr11:14520308-14520502 | Rare:61 | ||||
| chr11:18322128-18322317 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):2 |