| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108222549-108223128 | Common:1; Rare:190; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223274-108223859 | Common:2; Rare:144 | ||||
| chr11:108223973-108224101 | Rare:28 | ||||
| chr11:110296502-110296880 | Common:3; Rare:163; Clinvar:8 | ||||
| chr11:111364264-111364445 | Common:1; Rare:29 | ||||
| chr11:111379175-111379435 | Common:1; Rare:50 | ||||
| chr11:111379439-111379478 | Rare:14 | ||||
| chr11:111540445-111540739 | Common:1; Rare:74 | ||||
| chr11:111541484-111541560 | Common:2; Rare:17 | ||||
| chr11:111814616-111814911 | Common:1; Rare:46 | ||||
| chr11:111871243-111871380 | Common:1; Rare:44; Clinvar:1 | ||||
| chr11:111878705-111878973 | Common:2; Rare:72 | ||||
| chr11:111879152-111879548 | Common:1; Rare:121 | ||||
| chr11:111912729-111912774 | Rare:4 | ||||
| chr11:111913138-111913300 | Rare:45 |