| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35662671-35662953 | Common:7; Rare:194 | ||||
| chr11:35662970-35663360 | Rare:234 | ||||
| chr11:35943891-35944141 | Common:7; Rare:158 | ||||
| chr11:35944165-35944583 | Common:2; Rare:167 | ||||
| chr11:36289312-36289584 | Common:4; Rare:146 | ||||
| chr11:36376160-36376469 | Common:5; Rare:99 | ||||
| chr11:36510187-36510382 | Rare:114 | ||||
| chr11:43311816-43312629 | Common:8; Rare:381 | ||||
| chr11:43358756-43359310 | Rare:449 | ||||
| chr11:43680377-43680871 | Common:5; Rare:139 | ||||
| chr11:43680990-43681550 | Common:3; Rare:165 | ||||
| chr11:43880694-43880963 | Common:6; Rare:165 | ||||
| chr11:44065920-44066590 | Common:14; Rare:407 | ||||
| chr11:44095637-44095781 | Common:1; Rare:39; Clinvar (benign):2 | ||||
| chr11:44095870-44096527 | Common:9; Rare:312 |