| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9384512-9384807 | Common:3; Rare:177 | ||||
| chr11:9460609-9461044 | Common:8; Rare:219 | ||||
| chr11:9572920-9573270 | Common:5; Rare:119 | ||||
| chr11:9573320-9573816 | Common:5; Rare:286 | ||||
| chr11:9663898-9664188 | Common:8; Rare:152 | ||||
| chr11:10293701-10294101 | Common:6; Rare:173; Clinvar (pathogenic):1 | ||||
| chr11:10304520-10304760 | Common:4; Rare:86 | ||||
| chr11:10304777-10305089 | Common:2; Rare:115 | ||||
| chr11:10541138-10541331 | Rare:144 | ||||
| chr11:10751128-10751322 | Rare:94 | ||||
| chr11:10808752-10809218 | Common:5; Rare:322 | ||||
| chr11:10858004-10858282 | Common:5; Rare:168 | ||||
| chr11:11841060-11841600 | Common:9; Rare:151 | ||||
| chr11:11841655-11842121 | Common:5; Rare:181 | ||||
| chr11:12110343-12110602 | Rare:65 |