| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43359050-43359291 | Rare:79 | ||||
| chr11:43644153-43644270 | Rare:20 | ||||
| chr11:43680388-43680821 | Common:4; Rare:115 | ||||
| chr11:43880571-43880878 | Common:2; Rare:71 | ||||
| chr11:44066114-44066478 | Common:4; Rare:91 | ||||
| chr11:44565391-44565680 | Common:2; Rare:70 | ||||
| chr11:44726856-44727002 | Common:7; Rare:28 | ||||
| chr11:44949580-44949691 | Common:4; Rare:25 | ||||
| chr11:44949803-44950154 | Common:2; Rare:74 | ||||
| chr11:44950761-44951116 | Common:4; Rare:101 | ||||
| chr11:45146581-45147521 | Common:7; Rare:295 | ||||
| chr11:45665595-45665817 | Common:2; Rare:51 | ||||
| chr11:45804246-45804591 | Common:1; Rare:72 | ||||
| chr11:45804930-45805196 | Common:3; Rare:69; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847165-45847512 | Common:2; Rare:139 |