| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:83716090-83716360 | Common:2; Rare:59 | ||||
| chr11:86052851-86053590 | Common:4; Rare:289 | ||||
| chr11:86174245-86174534 | Common:2; Rare:89 | ||||
| chr11:86183020-86183380 | Common:3; Rare:130 | ||||
| chr11:86193301-86194083 | Common:11; Rare:228 | ||||
| chr11:86196270-86196710 | Common:4; Rare:160 | ||||
| chr11:86735748-86736377 | Common:10; Rare:289 | ||||
| chr11:86743390-86743740 | Common:4; Rare:109 | ||||
| chr11:86743730-86744110 | Rare:124 | ||||
| chr11:86776220-86776710 | Common:5; Rare:87 | ||||
| chr11:86956020-86956170 | Common:2; Rare:43 | ||||
| chr11:88312440-88312750 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr11:94732680-94732960 | Common:1; Rare:42 | ||||
| chr11:94746810-94747060 | Common:2; Rare:55 | ||||
| chr11:94747050-94747750 | Common:5; Rare:161 |