| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:308053-308408 | Common:9; Rare:120 | ||||
| chr11:320564-320936 | Common:5; Rare:143; Clinvar:1 | ||||
| chr11:450152-450318 | Rare:50 | ||||
| chr11:498822-499037 | Common:2; Rare:103 | ||||
| chr11:506356-506462 | Common:2; Rare:28 | ||||
| chr11:506728-507001 | Common:3; Rare:92 | ||||
| chr11:507113-507508 | Common:4; Rare:127 | ||||
| chr11:560706-561016 | Common:6; Rare:143 | ||||
| chr11:576412-576565 | Rare:65 | ||||
| chr11:615943-616043 | Common:1; Rare:31 | ||||
| chr11:695708-695821 | Rare:38 | ||||
| chr11:706013-706244 | Common:2; Rare:70 | ||||
| chr11:747284-747578 | Rare:125; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:763341-763854 | Rare:225; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr11:777451-777637 | Common:1; Rare:85 |