| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16613561-16613691 | Rare:25 | ||||
| chr11:16738397-16738560 | Common:2; Rare:44 | ||||
| chr11:16738561-16738967 | Common:1; Rare:105 | ||||
| chr11:17014394-17014743 | Common:6; Rare:128 | ||||
| chr11:17077417-17077864 | Common:4; Rare:170 | ||||
| chr11:17207846-17208149 | Common:2; Rare:107 | ||||
| chr11:17276084-17276384 | Common:3; Rare:69 | ||||
| chr11:17276557-17277060 | Common:5; Rare:120; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17351861-17352029 | Common:2; Rare:39 | ||||
| chr11:17544414-17544497 | Common:2; Rare:17 | ||||
| chr11:18012903-18013047 | Common:4; Rare:55 | ||||
| chr11:18322058-18322352 | Common:6; Rare:109; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322437-18322677 | Common:2; Rare:85 | ||||
| chr11:18394405-18394745 | Common:1; Rare:122; Clinvar (benign):1 | ||||
| chr11:18396153-18396410 | Common:1; Rare:100 |