| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:44095586-44095763 | Common:1; Rare:51; Clinvar (benign):2 | ||||
| chr11:44565082-44565749 | Common:5; Rare:165 | ||||
| chr11:44565843-44565912 | Common:1; Rare:9 | ||||
| chr11:44596690-44596831 | Rare:28 | ||||
| chr11:44597044-44597221 | Common:3; Rare:45 | ||||
| chr11:44726318-44726569 | Common:2; Rare:67 | ||||
| chr11:44726829-44726983 | Common:8; Rare:28 | ||||
| chr11:45146562-45146732 | Common:2; Rare:39 | ||||
| chr11:45147079-45147389 | Common:1; Rare:135 | ||||
| chr11:45804904-45805224 | Common:3; Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45805428-45805515 | Common:1; Rare:15; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:45847115-45847564 | Common:2; Rare:173 | ||||
| chr11:45917756-45918004 | Rare:67; Clinvar:4 | ||||
| chr11:45918098-45918274 | Rare:44 | ||||
| chr11:45918787-45918922 | Rare:39 |