| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43359342-43359380 | Rare:15 | ||||
| chr11:43644154-43644270 | Rare:20 | ||||
| chr11:43680305-43680893 | Common:6; Rare:169 | ||||
| chr11:43681022-43681310 | Common:2; Rare:50 | ||||
| chr11:43880637-43880967 | Common:2; Rare:87 | ||||
| chr11:43942525-43942654 | Rare:27 | ||||
| chr11:44065978-44066346 | Common:3; Rare:99 | ||||
| chr11:44066371-44066578 | Common:2; Rare:51 | ||||
| chr11:44095646-44095792 | Common:1; Rare:37; Clinvar (benign):2 | ||||
| chr11:44096114-44096217 | Rare:33 | ||||
| chr11:44096234-44096242 | |||||
| chr11:44565344-44565730 | Common:2; Rare:94 | ||||
| chr11:45146190-45146301 | Rare:26 | ||||
| chr11:45146509-45146735 | Common:2; Rare:60 | ||||
| chr11:45146773-45146960 | Common:2; Rare:46 |