| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:208615-208857 | Rare:88 | ||||
| chr11:236333-236559 | Common:8; Rare:73 | ||||
| chr11:320667-320936 | Common:5; Rare:108; Clinvar:1 | ||||
| chr11:506678-507021 | Common:3; Rare:106 | ||||
| chr11:560707-560987 | Common:6; Rare:129 | ||||
| chr11:706516-706647 | Rare:22 | ||||
| chr11:777465-777598 | Common:1; Rare:58 | ||||
| chr11:809269-809352 | Common:2; Rare:21 | ||||
| chr11:809865-810035 | Common:2; Rare:85 | ||||
| chr11:842500-842981 | Common:8; Rare:191 | ||||
| chr11:843871-844111 | Common:2; Rare:68 | ||||
| chr11:1309569-1309732 | Common:1; Rare:73 | ||||
| chr11:6481283-6481527 | Common:4; Rare:98 | ||||
| chr11:6603577-6603865 | Common:2; Rare:84; Clinvar (benign):3 | ||||
| chr11:8682641-8682811 | Common:2; Rare:75 |