| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9460682-9461038 | Common:4; Rare:95 | ||||
| chr11:9663894-9664174 | Common:4; Rare:86 | ||||
| chr11:10304812-10305078 | Common:1; Rare:57 | ||||
| chr11:10751163-10751305 | Rare:42 | ||||
| chr11:10808891-10809263 | Common:3; Rare:160 | ||||
| chr11:10858019-10858250 | Common:3; Rare:74 | ||||
| chr11:11841903-11842063 | Common:1; Rare:48 | ||||
| chr11:12377476-12377643 | Rare:67 | ||||
| chr11:13463147-13463395 | Common:1; Rare:92 | ||||
| chr11:14499757-14499922 | Common:2; Rare:58 | ||||
| chr11:14520297-14520549 | Rare:87 | ||||
| chr11:16738460-16738729 | Common:3; Rare:57 | ||||
| chr11:17207910-17208010 | Common:2; Rare:41 | ||||
| chr11:17276566-17276813 | Common:3; Rare:64; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:18322108-18322312 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):2 |